Substituted thiophenecarboxamides and analogues as antibacterials agents

ABSTRACT

The present disclosure relates to substituted thiophene carboxamides and analogues thereof of formula (I) that may be used for protecting plants from bacterial diseases, in particular from bacterial diseases caused by bacteria belonging to the genus  Xanthomonas .

CROSS REFERENCE TO RELATED APPLICATIONS

This application is a national stage application under 35 U.S.C. § 371of International Application No. PCT/EP2019/067824, filedinternationally on Jul. 3, 2019, which claims priority to and benefit ofEuropean Application No. 18181930.1, filed Jul. 5, 2018.

TECHNICAL FIELD

The present invention relates to substituted thiophene carboxamides andanalogues thereof that may be used for protecting plants from bacterialdiseases, in particular caused by bacteria belonging to the genusXanthomonas.

BACKGROUND

Plant pathogenic bacteria can cause severe economically damagingdiseases throughout the world. Bacteria belonging to the genusXanthomonas are among the plant pathogenic bacteria considered to be themost devastating. They are the causal agents of various diseases ondifferent host plants of agronomic significance. Examples of suchdiseases include bacterial spot (caused by Xanthomonas campestris pv.vesicatoria) affecting pepper and tomato, black rot of crucifers (causedby Xanthomonas campestris pv. campestris) affecting all cultivatedbrassica (e.g. Brussels sprouts, cabbage, cauliflower and broccoli),citrus canker (caused by Xanthomonas axonopodis pv. citri) affectingcitrus species (lime, orange, grapefruit, pummelo), bacterial leafblight (caused by Xanthomonas oryzae pv. oryzae) affecting rice, leafspot (caused by Xanthomonas arboricola pv. pruni) affecting Prunusspecies (e.g. apricot, plum, peach), common bacterial blight (caused byXanthomonas phaseoli) affecting bean, cassava bacterial blight (causedby Xanthomonas axonopodis pv. manihotis) affecting cassava and angularleaf spot/bacterial blight (cause by Xanthomonas campestris pv.malvacearum) affecting cotton.

Bacterial plant diseases may be controlled in different ways, includingmainly the use of disease-resistant varieties of plants and the use ofbactericides (natural or synthetic). The antibiotic resistance crisis inmedicine and the emergence of some antibiotic resistant plant pathogenshave triggered the development of alternatives to antibiotics in orderto preserve their efficacy and to broaden the scope of diseasemanagement solutions. Therefore, products that do not act directly onthe pathogenic bacteria, i.e. that have no direct antibiotic effect, butthat stimulate the plants' own defense system have been developed. Theseproducts are known as plant defense activators. Examples of plantdefense activators include Acibenzolar-S-methyl (marketed as Bion® andActigard®), 2, 6-dichloroisonicotinic acid, β-aminobutyric acid,probenazole (Oryzemate®), salicylic acid, riboflavin,prohexadione-calcium, potassium phosphonate, harpin protein (Messenger®)and methyl jasmonate.

Though many different organic and inorganic compounds have been shown toactivate induced resistance in plants, only few products are currentlycommercially marketed.

Therefore, the need remains to provide new chemicals and methodsallowing controlling efficiently bacterial diseases, in particulardiseases caused by bacteria belonging to the genus Xanthomonas, at lowdose while not interacting directly with the bacteria so as to preventresistance development. As the chemicals do not interact directly withthe bacteria, it is unlikely that they will develop resistance to thesechemicals.

The inventors have evidenced that new chemicals belonging to the classof substituted thiophenecarboxamides derivatives are offering a solutionto the above problem.

Some substituted thiophenecarboxamide derivatives are known to be usefulfor combatting plant diseases. For instance, U.S. Pat. No. 5,534,541 orEP0450355 discloses halogeno thiophene carboxylic acid derivatives thatare useful for protecting plants from attacks by plant-damagingmicroorganisms, such as fungi and bacteria, via a direct action or asystemic action. However, these compounds were found by the presentinventors to be poorly efficient against Xanthomonas campestris pv.campestris at low dose.

Further examples of halogeno thiophene carboxylic acid derivatives aredisclosed in WO2004/024692. These derivatives are said to be effectivein controlling fungal diseases. They would exert their action via adirect effect on the undesired microorganisms but also thanks to aresistance inducing effect on plants. WO2004/024692 also suggests thatthese compounds could be useful in controlling bacterial diseases butdoes not provide any evidences of such activity. These compounds werealso found by the present inventors to be poorly efficient againstXanthomonas campestris pv. campestris at low dose.

SUMMARY

The present invention relates to compounds of formula (I) as disclosedherein and in the claims.

The present invention also relates to a method for controlling bacterialdiseases as disclosed herein and in the claims.

The present invention relates to processes for preparing compounds offormula (I) and to intermediates thereof as disclosed herein and in theclaims.

Definitions

The term “C₁-C₆-alkyl” as used herein refers to a saturated, branched orstraight hydrocarbon chain having 1, 2, 3, 4, 5 or 6 carbon atoms.Examples of C₁-C₆-alkyl include but are not limited to methyl, ethyl,propyl (n-propyl), 1-methylethyl (iso-propyl), butyl (n-butyl),1-methylpropyl (sec-butyl), 2-methylpropyl (iso-butyl),1,1-dimethylethyl (tert-butyl), pentyl, 1-methylbutyl, 2-methylbutyl,3-methylbutyl, 2,2-dimethylpropyl, 1-ethylpropyl, 1,1-dimethylpropyl,1,2-dimethylpropyl, hexyl, 1-methylpentyl, 2-methylpentyl,3-methylpentyl, 4-methylpentyl, 1,1-dimethylbutyl, 1,2-dimethylbutyl,1,3-dimethylbutyl, 2,2-dimethylbutyl, 2,3-dimethylbutyl,3,3-dimethylbutyl, 1-ethylbutyl, 2-ethylbutyl, 1,1,2-trimethylpropyl,1,2,2-trimethylpropyl, 1-ethyl-1-methylpropyl and1-ethyl-2-methylpropyl. Particularly, said hydrocarbon chain has 1, 2, 3or 4 carbon atoms (“C₁-C₄-alkyl”), e.g. methyl, ethyl, propyl,iso-propyl, butyl, sec-butyl, iso-butyl or tert-butyl.

The term “alkenyl” as used herein is to be understood as preferablymeaning branched and unbranched alkenyl, e.g. a vinyl, propen-1-yl,propen-2-yl, but-1-en-1-yl, but-1-en-2-yl, but-2-en-1-yl, but-2-en-2-yl,but-1-en-3-yl, 2-methyl-prop-2-en-1-yl, or 2-methyl-prop-1-en-1-ylgroup.

The term “alkynyl” as used herein is to be understood as preferablymeaning branched and unbranched alkynyl, e.g. an ethynyl,prop-1-yn-1-yl, but-1-yn-1-yl, but-2-yn-1-yl, or but-3-yn-1-yl group.The term “C₁-C₆-alkylsulfanyl” as used herein refers to a saturated,linear or branched group of formula (C₁-C₆-alkyl)-S—, in which the term“C₁-C₆-alkyl” is as defined herein. Examples of C₁-C₆-alkylsulfanylinclude but are not limited to methylsulfanyl, ethylsulfanyl,propylsulfanyl, isopropylsulfanyl, butylsulfanyl, sec-butylsulfanyl,isobutylsulfanyl, tert-butylsulfanyl, pentylsulfanyl, isopentylsulfanyl,hexylsulfanyl group.

The term “aryl” as used herein refers to an aromatic, hydrocarbon, ringsystem, comprising from 6 to 12 carbon atoms, preferably from 6 to 10carbon atoms. The ring system may be monocyclic or fused polycyclic(e.g. bicyclic or tricyclic) aromatic ring system. Examples of arylinclude but are not limited to phenyl, azulenyl, naphthyl, biphenyl andfluorenyl.

The term “aralkyl” as used herein refers to a C₁-C₆-alkyl substituted byan aryl as defined herein. Example of aralkyl includes the benzyl group(—CH₂—C₆H₅).

The term “cycloalkyl” as used herein refers to a non-aromatic monocycliccarbon-containing ring, having 3 to 8 carbon atoms. Examples ofsaturated cycloalkyl include but are not limited to cyclopropyl,cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, cyclononyland cyclodecyl group.

The term “heterocyclyl” as used herein refers to four-, five- orsix-membered, saturated or partially unsaturated heterocycles containingone to four heteroatoms independently selected from the group of oxygen,nitrogen and sulfur. If the ring contains more than one oxygen atom,they are not directly adjacent.

The term “aryl” as used herein refers to an aromatic, hydrocarbon, ringsystem, comprising from 6 to carbon atoms, or from 6 to 12 carbon atoms,preferably from 6 to 10 carbon atoms. The ring system may be monocyclicor fused polycyclic (e.g. bicyclic or tricyclic) aromatic ring system.

Examples of aryl include but are not limited to phenyl, azulenyl,naphthyl and fluorenyl. It is further understood that when said arylgroup is substituted with one or more substituents, said substituent(s)may be at any positions on said aryl ring(s). Particularly, in the caseof aryl being a phenyl group, said substituent(s) may occupy one or bothortho positions, one or both meta positions, or the para position, orany combination of these positions. This definition also applies to arylas part of a composite substituent (e.g. aryloxy).

DETAILED DESCRIPTION

Compounds of formula (I) as shown below have been found to efficientlycontrol diseases caused by bacteria of the genus Xanthomonas at low dose(i.e. dose as low as 31 ppm) while exhibiting no direct bactericideaction.

Thus, the present invention relates to compounds of the formula (I):

whereinR¹ and R² are identical and are a chlorine atom or a bromine atom;R³ is methyl;R⁴ is selected from the group consisting of hydrogen atom, C₁-C₆-alkyl,aralkyl, aralkyl substituted by hydroxyl, C₁-C₆-alkyl substituted by aC₁-C₆-alkylsulfanyl and R⁵ is a hydrogen atom; orR⁴ and R⁵ form, together with the carbon atom to which they are linked,a cyclopropyl;R⁶ is selected from the group consisting of hydrogen atom, C₁-C₆-alkyl,C₁-C₆-haloalkyl, C₁-C₆-cyanoalkyl, C₂-C₆-alkenyl, C₂-C₆-alkynyl,C₃-C₈-cycloalkyl, aryl, aralkyl, 4-, 5- or 6-membered heterocyclyl,—C₁-C₆-alkyl-Si(C₁-C₆-alkyl)₃ and —C₁-C₆-alkyl-C₃-C₈-cycloalkyl.

The invention encompasses pure stereoisomers of the compound of formula(I) and any mixture of these isomers.

Not encompassed herein are compounds resulting from combinations whichare against natural laws and which the person skilled in the art wouldtherefore exclude based on his/her expert knowledge. For instance, ringstructures having three or more adjacent oxygen atoms are excluded.

Depending on the nature of the substituents, the compound of formula (I)may be present in the form of different stereoisomers. Thesestereoisomers are, for example, enantiomers, diastereomers, atropisomersor geometric isomers. Accordingly, the invention encompasses both purestereoisomers and any mixture of these isomers. Where a compound can bepresent in two or more tautomer forms in equilibrium, reference to thecompound by means of one tautomeric description is to be considered toinclude all tautomer forms.

Any of the compounds of the present invention can also exist in one ormore geometric isomer forms depending on the number of double bonds inthe compound. Geometric isomers by nature of substituents about a doublebond or a ring may be present in cis (=Z-) or trans (=E-) form. Theinvention thus relates equally to all geometric isomers and to allpossible mixtures, in all proportions.

The compound of formula (I) can suitably be in its free form, salt form,N-oxide form or solvate form (e.g. hydrate).

Depending on the nature of the substituents, the compound of formula (I)may be present in the form of the free compound and/or a salt thereof,such as an agrochemically active salt.

Agrochemically active salts include acid addition salts of inorganic andorganic acids well as salts of customary bases. Examples of inorganicacids are hydrohalic acids, such as hydrogen fluoride, hydrogenchloride, hydrogen bromide and hydrogen iodide, sulfuric acid,phosphoric acid and nitric acid, and acidic salts, such as sodiumbisulfate and potassium bisulfate. Useful organic acids include, forexample, formic acid, carbonic acid and alkanoic acids such as aceticacid, trifluoroacetic acid, trichloroacetic acid and propionic acid, andalso glycolic acid, thiocyanic acid, lactic acid, succinic acid, citricacid, benzoic acid, cinnamic acid, oxalic acid, saturated or mono- ordiunsaturated fatty acids having 6 to 20 carbon atoms, alkylsulfuricmonoesters, alkylsulfonic acids (sulfonic acids having straight-chain orbranched alkyl radicals having 1 to 20 carbon atoms), arylsulfonic acidsor aryldisulfonic acids (aromatic radicals, such as phenyl and naphthyl,which bear one or two sulfonic acid groups), alkylphosphonic acids(phosphonic acids having straight-chain or branched alkyl radicalshaving 1 to 20 carbon atoms), arylphosphonic acids or aryldiphosphonicacids (aromatic radicals, such as phenyl and naphthyl, which bear one ortwo phosphonic acid radicals), where the alkyl and aryl radicals maybear further substituents, for example p-toluenesulfonic acid, salicylicacid, p-aminosalicylic acid, 2-phenoxybenzoic acid, 2-acetoxybenzoicacid, etc.

Solvates of the compounds of formula (I) or their salts arestoichiometric compositions of the compounds with solvents.

The compounds of formula (I) may exist in multiple crystalline and/oramorphous forms. Crystalline forms include unsolvated crystalline forms,solvates and hydrates.

In some embodiments, in the above formula (I), R⁴ is selected from thegroup consisting of hydrogen atom, C₁-C₆-alkyl, benzyl, benzylsubstituted by hydroxyl, C₁-C₆-alkyl substituted by aC₁-C₆-alkylsulfanyl and R⁵ is a hydrogen atom; or R⁴ and R⁵ form,together with the carbon atom to which they are linked, a cyclopropyl.

In some embodiments, in the above formula (I), R⁴ is selected from thegroup consisting of hydrogen atom, C₁-C₆-alkyl, benzyl, benzylsubstituted by hydroxyl, C₁-C₆-alkyl substituted by aC₁-C₆-alkylsulfanyl and R⁵ is a hydrogen atom.

In some embodiments, in the above formula (I), R⁴ is a hydrogen atom, aC₁-C₆-alkyl, an aralkyl or a C₁-C₆-alkyl substituted by aC₁-C₆-alkylsulfanyl and R⁵ is a hydrogen atom; or R⁴ and R⁵ form,together with the carbon atom to which they are linked, a cyclopropyl.

In some embodiments, in the above formula (I), R⁴ is a hydrogen atom, aC₁-C₆-alkyl, an aralkyl or a C₁-C₆-alkyl substituted by aC₁-C₆-alkylsulfanyl and R⁵ is a hydrogen atom.

Non-limiting examples of suitable R⁴ groups include any of the R⁴ groupsdisclosed in column “R⁴” of Table I.1.

In some embodiments, in the above formula (I), R⁶ is selected from thegroup consisting of hydrogen atom, C₁-C₆-alkyl, C₁-C₆-haloalkyl,C₁-C₆-cyanoalkyl, C₂-C₆-alkenyl, C₂-C₆-alkynyl, C₃-C₈-cycloalkyl,phenyl, benzyl, 4-, 5- or 6-membered heterocyclyl,—C₁-C₆-alkyl-Si(C₁-C₆-alkyl)₃ and —C₁-C₆-alkyl-cyclopropyl.

When R⁶ is a 4-, 5- or 6-membered heterocyclyl, it may be a saturated orpartially unsaturated heterocyclyl. Examples of saturated 4-, 5- or6-membered heterocyclyl include but are not limited to 4-membered ringsuch as azetidinyl, oxetanyl, thietanyl, dioxothietanyl, 5-membered ringsuch as oxolanyl, 1,3-dioxolanyl, tetrahydrothienyl, pyrrolidinyl,pyrazolidinyl, imidazolidinyl, triazolidinyl, isoxazolidinyl,oxazolidinyl, oxadiazolidinyl, thiazolidinyl, isothiazolidinyl,thiadiazolidinyl, 6-membered ring such as piperidinyl,hexahydropyridazinyl, hexahydropyrimidinyl, piperazinyl, triazinanyl,hexahydrotriazinyl, oxanyl, dioxanyl, tetrahydrothiopyranyl, dithianyl,morpholinyl, 1,2-oxazinanyl, oxathianyl, thiomorpholinyl. Examples ofpartially unsaturated non-aromatic hererocyles include but are notlimited to 5-membered ring such as dihydrofuranyl, 1,3-dioxolyl,dihydrothienyl, pyrrolinyl, dihydroimidazolyl, dihydropyrazolyl,isoxazolinyl, dihydrooxazolyl, dihydrothiazolyl or 6-membered ring suchas pyranyl, thiopyranyl, thiazinyl and thiadiazinyl.

In some embodiments, in the above formula (I), R⁶ is selected from thegroup consisting of hydrogen atom, C₁-C₆-alkyl, C₁-C₆-haloalkyl,C₁-C₆-cyanoalkyl, C₂-C₆-alkenyl, C₂-C₆-alkynyl, C₃-C₈-cycloalkyl,phenyl, benzyl, oxetanyl, thietanyl, dioxothietanyl, oxolanyl, oxanyl,—C₁-C₆-alkyl-Si(C₁-C₆-alkyl)₃ and —C₁-C₆-alkyl-cyclopropyl.

In some embodiments, in the above formula (I), R⁶ is a hydrogen atom ora C₁-C₆-alkyl.

Non-limiting examples of suitable R⁶ groups include any of the R⁶ groupsdisclosed in column “R⁶” of Table I.1.

In some embodiments, in the above formula (I), R¹ and R² are a chlorineatom.

In some embodiments, in the above formula (I), R¹ and R² are a bromineatom.

The above specified definitions of R¹, R², R⁴ and R⁶ and can be combinedin various manners to provide sub-classes of compounds according to theinvention.

Non-limiting examples of sub-classes of compounds include thesub-classes described herein below.

In some embodiments (referred herein as embodiment Ia), compounds of theinvention are compounds of formula (I):

whereinR¹ and R² are identical and are a chlorine atom or a bromine atom;R³ is methyl;R⁴ is selected from the group consisting of hydrogen atom, C₁-C₆-alkyl,benzyl, benzyl substituted by hydroxyl, C₁-C₆-alkyl substituted by aC₁-C₆-alkylsulfanyl and R⁵ is a hydrogen atom; orR⁴ and R⁵ form, together with the carbon atom to which they are linked,a cyclopropyl;R⁶ is selected from the group consisting of hydrogen atom, C₁-C₆-alkyl,C₁-C₆-haloalkyl, C₁-C₆-cyanoalkyl, C₂-C₆-alkenyl, C₂-C₆-alkynyl,C₃-C₈-cycloalkyl, phenyl, benzyl, oxetanyl, thietanyl, dioxothietanyl,oxolanyl, oxanyl, —C₁-C₆-alkyl-Si(C₁-C₆-alkyl)₃ and—C₁-C₆-alkyl-cyclopropyl.

In some embodiments (referred herein as embodiment Ib), compounds of theinvention are compounds of formula (I):

whereinR¹ and R² are identical and are a chlorine atom or a bromine atom;R³ is methyl;R⁴ is a hydrogen atom, a C₁-C₆-alkyl, an aralkyl or a C₁-C₆-alkylsubstituted by a C₁-C₆-alkylsulfanyl and R⁵ is a hydrogen atom; orR⁴ and R⁵ form, together with the carbon atom to which they are linked,a cyclopropyl;R⁶ is a hydrogen atom or a C₁-C₆-alkyl.

In some embodiments in accordance with embodiments Ia and Ib, when R⁴and R⁵ do not form, together with the carbon atom to which they arelinked, a cyclopropyl, R⁴ is preferably a hydrogen atom, a C₁-C₄-alkyl,a benzyl group or a C₁-C₄-alkyl substituted by a C₁-C₄-alkylsulfanyl,more preferably R⁴ is hydrogen, isopropyl, isobutyl, methylsulfanylethylor benzyl.

In some embodiments in accordance with embodiments Ia and Ib, R⁶ is ahydrogen atom or a C₁-C₄-alkyl, preferably R⁶ is hydrogen, methyl orethyl.

In some embodiments in accordance with embodiments Ia and Ib, R¹ and R²are a chlorine atom. In some embodiments in accordance with embodimentsIa and Ib, R¹ and R² are a bromine atom.

In some embodiments in accordance with embodiments Ia and Ib, when R¹and R² are a bromine atom, R⁴ is a hydrogen atom, a C₁-C₆-alkyl, anaralkyl or a C₁-C₆-alkyl substituted by a C₁-C₆-alkylsulfanyl and R⁵ isa hydrogen atom.

In some embodiments, compounds according to the present invention arecompounds of the formula (I):

whereinR¹ and R² are identical and are a chlorine atom or a bromine atom;R³ is methyl;R⁴ is a hydrogen atom, a C₁-C₄-alkyl, a benzyl group or a C₁-C₄-alkylsubstituted by a C₁-C₄-alkylsulfanyl, preferably R⁴ is hydrogen,isopropyl, isobutyl, methylsulfanylethyl or benzyl and R⁵ is a hydrogenatom; orR⁴ and R⁵ form, together with the carbon atom to which they are linked,a cyclopropyl;R⁶ is a hydrogen atom or a C₁-C₄-alkyl, preferably R⁶ is hydrogen,methyl or ethyl.

The compounds of formula (I) may be used for controlling bacterialdiseases, in particular for controlling diseases caused by bacteriabelonging to the genus Xanthomonas.

Processes for the Preparation of Compounds of Formula (I)

The present invention relates to processes for the preparation ofcompounds of formula (I). The compounds of formula (I) can be preparedby various routes in analogy to known processes (see referencestherein), and by one or more of the following synthetic routes describedherein below and in the experimental part.

General Synthetic Routes to the Compounds of Formula (I)

Unless indicated otherwise, in the following, R¹, R², R³, R⁴, R⁵ and R⁶have the same meaning as given above for compounds of formula (I).

Process A1

Compounds of formula (I) as herein-defined can be prepared by a processA1 which comprises the step of reacting a compound of formula (IV) orone of its salts with a compound of formula (V) or one of its salts asillustrated by the following reaction scheme:

wherein U¹ is a halogen atom, a hydroxy group or a C₁-C₆-alkoxy group.

When U¹ represents a hydroxy group, process A1 is advantageouslyconducted in the presence of a condensing agent. Suitable condensingagents may be selected in the non-limited list consisting of acid halideformer, such as phosgene, phosphorous tribromide, phosphoroustrichloride, phosphorous pentachloride, phosphorous trichloride oxide,oxalyl chloride or thionyl chloride; anhydride former, such as ethylchloroformate, methyl chloroformate, isopropyl chloroformate, isobutylchloroformate or methanesulfonyl chloride; carbodiimides, such asN,N′-dicyclohexylcarbodiimide (DCC),N-(3-Dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (EDC) orother customary condensing agents, such as phosphorous pentoxide,polyphosphoric acid, bis(2-oxo-3-oxazolidinyl)phosphinic chloride,1-[bis(dimethylamino)methylene]-1H-1,2,3-triazolo[4,5-b]pyridinium3-oxid hexafluorophosphate (HATU),2-(1H-Benzotriazole-1-yl)-1,1,3,3-tetramethylaminium tetrafluoroborate(TBTU),(1-cyano-2-ethoxy-2-oxoethylidenaminooxy)dimethylamino-morpholino-carbeniumhexafluorophosphate, N,N′-carbonyl-diimidazole,2-ethoxy-N-ethoxycarbonyl-1,2-dihydroquinoline (EEDQ),triphenylphosphine/tetrachloro-methane,4-(4,6-dimethoxy[1.3.5]-triazin-2-yl)-4-methylmorpholinium chloridehydrate, bis(2-oxo-3-oxazolidinyl)phosphinic chloride (BOP-Cl),bromo-tripyrrolidinophosphoniumhexafluorophosphate (PyBroP),2-chloro-1,3-dimethylimidazolinium chloride (DMC) and propanephosphonicanhydride (T3P).

When U¹ represents a halogen atom, process A1 is advantageouslyconducted in the presence of an acid binder. Suitable acid binders forcarrying out process A1 are in each case all inorganic and organic basesthat are customary for such reactions. Preference is given to alkalimetal carbonates, such as cesium carbonate, sodium carbonate, potassiumcarbonate, potassium bicarbonate, sodium bicarbonate, alkaline earthmetal acetates, such as sodium acetate, potassium acetate, calciumacetate and also tertiary amines, such as trimethylamine, triethylamine,diisopropylethylamine, tributylamine, N,N-dimethylaniline,N-methylpiperidine, N,N-dimethylpyridin-4-amine, diazabicyclooctane(DABCO), diazabicyclo-nonene (DBN) or diazabicycloundecene (DBU), oraromatic bases such as pyridine.

When U¹ represents a C₁-C₆-alkoxy group, process A1 can be conductedwith an excess of the amine component, optionally in the presence of aLewis acid such as trimethylaluminium.

If appropriate, process A1 can be performed in the presence of a baseand if appropriate, in the presence of a solvent, preferably underanhydrous conditions.

Suitable solvents for carrying out process A1 are not particularlylimited. They can be customary inert organic solvents as long as it isnot dissolving the compound to react therewith or exhibit any particularinteraction therewith. Preference is given to using optionallyhalogenated, aliphatic, alicyclic or aromatic hydrocarbons, such aspetroleum ether, pentane, hexane, heptane, cyclohexane,methylcyclohexane, benzene, toluene, xylene, decalin, ISOPAR™ E orISOPAR™ G, chlorobenzene, dichlorobenzene, dichloromethane, chloroform,carbon tetrachloride, 1,2-dichloroethane or trichloroethane; ethers,such as diethyl ether, diisopropyl ether, methyl tert-butyl ether,methyl tert-amyl ether, dioxane, tetrahydrofuran,2-methyltetrahydrofuran, 1,2-dimethoxyethane, 1,2-diethoxyethane oranisole; nitriles, such as acetonitrile, propionitrile, n- oriso-butyronitrile or benzonitrile; amides, such asN,N-dimethylformamide, N,N-dimethylacetamide, N-methylformanilide,N-methylpyrrolidone or hexamethylphosphoric triamide; ureas, such as1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone; esters, such asmethyl acetate or ethyl acetate, sulfoxides, such as dimethyl sulfoxide,or sulfones, such as sulfolane; and a mixture thereof.

Process A1 may be performed in an inert atmosphere such as argon ornitrogen atmosphere. When carrying out process A1, 1 mole or an excessof compound of formula (V) and from 1 to 5 moles of base can be employedper mole of compound of formula (IV). It is also possible to employ thereaction components in other ratios. Work-up is carried out by knownmethods.

Compounds of formula (V) are commercially available or can be preparedby well-known processes.

Compounds of formula (IV) wherein U¹ represents a hydroxy group arecommercially available, can be prepared from compounds of formula (IV)wherein U¹ represents a C₁-C₆-alkoxy group by well-known processes suchas basic hydrolysis or can be prepared by known processes (Beilstein J.Org. Chem. 2007, 3, No. 23)

Compounds of formula (IV) wherein U¹ represents a halogen arecommercially available or can be prepared from compounds of formula (IV)wherein U¹ represents a hydroxy group by well-known processes.

Compounds of formula (IV) wherein U¹ represents a C₁-C₆-alkoxy group canbe prepared from compounds of formula (IV) wherein U¹ represents ahydroxy group by well-known processes.

Process B1

Compounds of formula (I) as herein-defined can be prepared by a processB1 which comprises the step of reacting a compound of formula (VI) orone of its salts with a compound of formula (VII) or one of its salts asillustrated by the following reaction scheme:

wherein U² is a bromine atom, an iodine atom, a mesylate group, atosylate group or a triflate group and U³ is a boron derivative such asa boronic acid, a boronic ester derivative, a potassium trifluoroboratederivative or a halogenometal that can be complexed by 1 to 2 ligandssuch as a halogenomagnesium or a halogenozinc,provided that when R¹ and R² are bromine atoms, U² is not a bromineatom.

Process B1 can be performed in the presence of a transition metalcatalyst such as palladium and if appropriate, in the presence of aphosphine ligand or a N-heterocyclic carbene ligand, if appropriate, inthe presence of a base and if appropriate, in the presence of a solventaccording to known processes (WO2012054721, Angew. Chem. Int. Ed. 2017,56, 1581, Angew. Chem. Int. Ed. 2017, 56, 7078, and cited referencestherein).

Process B1 can be carried out in the presence of a catalyst, such as ametal salt or complex. Suitable metal derivatives for this purpose aretransition metal catalysts such as palladium. Suitable metal salts orcomplexes for this purpose are for example, palladium chloride,palladium acetate, tetrakis(triphenylphosphine)palladium(0),bis(dibenzylideneacetone)palladium(0),tris(dibenzylideneacetone)dipalladium(0),bis(triphenylphosphine)palladium(II) dichloride,[1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II),bis(cinnamyl)dichlorodipalladium(II),bis(allyl)-dichlorodipalladium(II),[1,1′-Bis(di-tert-butylphosphino)ferrocene]dichloropalladium(II),di-p-iodobis(tri-tert-butylphosphino)dipalladium(I) ordi-p-bromobis(tri-tert-butylphosphino)dipalladium(I).

It is also possible to generate a palladium complex in the reactionmixture by separate addition to the reaction of a palladium salt and aligand or salt, such as triethylphosphine, tri-tert-butylphosphine,tri-tert-butylphosphonium tetrafluoroborate, tricyclohexylphosphine,2-(dicyclohexylphosphino)biphenyl, 2-(di-tert-butylphosphino)biphenyl,2-(dicyclohexylphosphino)-2′-(N,N-dimethylamino)biphenyl,2-(tert-butylphosphino)-2′-(N,N-dimethylamino)biphenyl,2-di-tert-butylphosphino-2′,4′,6′-triisopropylbiphenyl2-dicyclohexylphosphino-2′,4′,6′-triisopropylbiphenyl,2-dicyclohexylphosphino-2,6′-dimethoxybiphenyl,2-dicyclohexylphosphino-2′,6′-diisopropoxybiphenyl, triphenyl-phosphine,tris-(o-tolyl)phosphine, sodium 3-(diphenylphosphino)benzenesulfonate,tris-2-(methoxy-phenyl)phosphine,2,2′-bis(diphenylphosphino)-1,1′-binaphthyl,1,4-bis(diphenylphosphino)butane, 1,2-bis(diphenylphosphino) ethane,1,4-bis(dicyclohexylphosphino)butane,1,2-bis(dicyclohexylphosphino)-ethane,2-(dicyclohexylphosphino)-2′-(N,N-dimethylamino)-biphenyl,1,1′-bis(diphenylphosphino)-ferrocene,(R)-(−)-1-[(S)-2-diphenyl-phosphino)ferrocenyl]ethyldicyclohexylphosphine,tris-(2,4-tert-butyl-phenyl)phosphite,di(1-adamantyl)-2-morpholinophenylphosphine or1,3-bis(2,4,6-trimethylphenyl)imidazolium chloride.

It is also advantageous to choose the appropriate catalyst and/or ligandfrom commercial catalogues such as “Metal Catalysts for OrganicSynthesis” by Strem Chemicals or “Phosphorous Ligands and Compounds” byStrem Chemicals.

Suitable bases for carrying out process B1 can be inorganic and organicbases which are customary for such reactions. Preference is given tousing alkaline earth metal or alkali metal hydroxides, such as sodiumhydroxide, calcium hydroxide, potassium hydroxide or other ammoniumhydroxide derivatives; alkaline earth metal, alkali metal or ammoniumfluorides such as potassium fluoride, cesium fluoride ortetrabutylammonium fluoride; alkaline earth metal or alkali metalcarbonates, such as sodium carbonate, potassium carbonate, potassiumbicarbonate, sodium bicarbonate or cesium carbonate; alkali metal oralkaline earth metal acetates, such as sodium acetate, lithium acetate,potassium acetate or calcium acetate; alkali metal or alkaline earthmetal phosphate, such as tripotassium phosphate alkali; alkali metalalcoholates, such as potassium tert-butoxide or sodium tert-butoxide;tertiary amines, such as trimethylamine, triethylamine, tributylamine,N,N-dimethylaniline, N,N-dicyclohexylmethylamine,N,N-diisopropylethylamine, N-methylpiperidine,N,N-dimethylaminopyridine, diazabicyclooctane (DABCO),diazabicyclononene (DBN) or diazabicycloundecene (DBU); and alsoaromatic bases, such as pyridine, picolines, lutidines or collidines.

Suitable solvents for carrying out process B1 can be customary inertorganic solvents. Preference is given to using optionally halogenatomated aliphatic, alicyclic or aromatic hydrocarbons, such aspetroleum ether, pentane, hexane, heptane, cyclohexane,methylcyclohexane, benzene, toluene, xylene or decalin; chlorobenzene,dichlorobenzene, dichloromethane, chloroform, carbon tetrachloride,dichloroethane or trichloroethane; ethers, such as diethyl ether,diisopropyl ether, methyl tert-butyl ether, methyl tert-amyl ether,dioxane, tetrahydrofuran, 2-methyltetrahydrofuran, 1,2-dimethoxyethane,1,2-diethoxyethane or anisole; nitriles, such as acetonitrile,propionitrile, n- or iso-butyronitrile or benzonitrile; amides, such asN,N-dimethylformamide, N,N-dimethylacetamide, N-methylformanilide,N-methylpyrrolidone or hexamethylphosphoric triamide; ureas, such as1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone; esters, such asmethyl acetate or ethyl acetate, sulfoxides, such as dimethyl sulfoxide,or sulfones, such as sulfolane; and a mixture thereof.

It can also be advantageous to carry out process B1 with a co-solventsuch as water or an alcohol such as methanol, ethanol, propanol,isopropanol or tert-butanol.

Process B1 may be performed in an inert atmosphere such as argon ornitrogen atmosphere. When carrying out process B1, 1 mole or an excessof compound of formula (VII) and from 1 to 5 moles of base and from 0.01to 20 mole percent of a palladium complex can be employed per mole ofcompound of formula (VI). It is also possible to employ the reactioncomponents in other ratios. Work-up is carried out by known methods.

Compounds of formula (VII) are commercially available or can be preparedby well-known processes.

Compounds of formula (VI) can be prepared by reacting a compound offormula (VIII) with a compound of formula (V) in the conditions asdescribed in connection with process A1:

wherein U² and U¹ are as herein-defined.

Compounds of formula (VIII) wherein U² is chlorine atom, a bromine atomor an iodine atom are commercially available or can be prepared bywell-known processes with the similar reaction conditions than the onesdisclosed to prepare compounds of formula (IV).

Compounds of formula (VIII) wherein U² is a mesylate group, a tosylategroup or a triflate group can be prepared by well-known processes fromthe corresponding compound bearing a hydroxy group at the U₂ position.

Process C1

Compounds of formula (I) as herein defined can be prepared by a processC1 from a compound of formula (IX) or one of its salts by performing abromination or chlorination reaction as illustrated in the followingreaction scheme:

wherein U⁴ is a hydrogen atom, a chlorine atom or a bromine atom and U⁵is a hydrogen atom, a chlorine atom or a bromine atom provided that atleast one of U⁴ or U⁵ is a hydrogen atom.

Process C1 can be carried out according to known processes(WO2008109786, WO2007098356).

Process C1 is performed in the presence of a bromination agent or achlorination agent and if appropriate, in the presence of a solvent.

Suitable bromination or chlorination agents for carrying out process C1are not particularly limited provided they are used for bromination orchlorination. Examples of bromination agents include bromine,N-bromosuccinimide and 1,3-dibromo-5,5-dimethyl-2,4-imidazolidinedione.Examples of chlorination agents include N-chlorosuccinimide, sulfurylchloride and 1,3-dichloro-5,5-dimethyl-2,4-imidazolidinedione.

Suitable solvents for carrying out process C1 are not particularlylimited. They can be customary inert organic solvents as long as it isnot dissolving the compound to react therewith or exhibit any particularinteraction therewith. Suitable solvents can be for instance thesolvents disclosed in connection with process A1. To carry out processC1, it can also be advantageous to use an organic acid such as aceticacid as a solvent or a co-solvent.

Process D1

Compounds of formula (I) as herein-defined can be prepared by a processD1 comprising the step of performing a diazotation of a compound offormula (X) or one of its salts followed by an aromatic substitution toprovide a compound of formula (I) as illustrated in the followingreaction scheme:

wherein U⁶ is an amino group, a chlorine atom or a bromine atom and U⁷is an amino group, a chlorine atom or a bromine atom provided that atleast one of U⁶ or U⁷ is an amino group.

Process D1 can be carried out according to known processes (TheChemistry of diazonium and diazo groups; Saul Patai; Wiley-Interscience;1978; 288-280 and 645-657; Account of Chemical Research (2018), 57, 496and cited references therein).

Compounds of formula (X) or one of its salts as herein-defined can beprepared by a process comprising the step of deprotecting a compound offormula (XI) or one of its salts as illustrated in the followingreaction scheme:

wherein U⁸ is a protected amino group, a chlorine atom or a bromine atomand U⁷ is a protected amino group, a chlorine atom or a bromine atomprovided that at least one of U⁸ or U⁹ is a protected amino group, U⁶ isan amino group, a chlorine atom or a bromine atom and U⁷ is an aminogroup, a chlorine atom or a bromine atom provided that at least one ofU⁶ or U⁷ is an amino group.

Examples of protecting groups of the amino group include a benzyl group,a 4-methoxybenzyl group, an allyl group, an unsubstituted or substitutedC₁-C₆-alkylsulfonyl, a trifluoromethylsulfonyl, an unsubstituted orsubstituted phenylsulfonyl, an unsubstituted or substitutedC₁-C₆-alkoxycarbonyl, an unsubstituted or substituted benzyloxycarbonyl,an allyloxycarbonyl, an acetyl group or a trifluoroacetyl group.

The deprotection process can be carried out according to known processesfor removing protecting groups (Greene's Protective Groups in OrganicSynthesis; Peter G. M. Wuts; Wiley; Fifth Edition; 2014; 895-1194). Forexample, tert-butoxycarbonyl and benzyloxycarbonyl protecting groups canbe removed in an acidic medium (for example with hydrochloric acid ortrifluoroacetic acid). Benzylic protecting groups can be removedhydrogenolytically with hydrogen in the presence of a catalyst (forexample palladium on activated carbon). Trifluoroacetyl group can beremoved in a basic medium (for example with potassium carbonate orlithium hydroxide).

Compounds of formula (X) can be prepared from compounds of formula (XII)or one of its salts and compounds of formula (XI) can be prepared fromcompounds of formula (XIII) or one of its salts by reaction with acompound of formula (V) in the conditions as described in process A1:

wherein U⁶, U⁷, U⁸ and U⁹ are as herein-defined, U¹ is a halogen atom, ahydroxy group or a C₁-C₆-alkoxy group.

Compounds of formula (XII) and compounds of formula (XIII) arecommercially available or can be prepared by well-known processes withthe similar reactions conditions than the ones disclosed to preparecompounds of formula (IV).

Compounds of formula (I) or one of its salts wherein R⁶ represents ahydrogen atom can be prepared from compounds of formula (I) wherein R⁶represents C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-cyanoalkyl,C₂-C₆-alkenyl, C₂-C₆-alkynyl, C₃-C₈-cycloalkyl, aryl, aralkyl, 4-, 5- or6-membered heterocyclyl, —C₁-C₆-alkyl-Si(C₁-C₆-alkyl)₃ or—C₁-C₆-alkyl-cyclopropyl by well-known processes such as basichydrolysis.

Compounds of formula (I) wherein R⁶ represents C₁-C₆-alkyl,C₁-C₆-haloalkyl, C₁-C₆-cyanoalkyl, C₂-C₆-alkenyl, C₂-C₆-alkynyl,C₃-C₈-cycloalkyl, aryl, aralkyl, 4-, 5- or 6-membered heterocyclyl,—C₁-C₆-alkyl-Si(C₁-C₆-alkyl)₃ or —C₁-C₆-alkyl-cyclopropyl can beprepared from compounds of formula (I) or one of its salts wherein R⁶represents a hydrogen atom by well-known processes.

The intermediates as disclosed herein may be efficient in controllingbacteria and/or fungi.

Intermediates for the Preparation of Compounds of Formula (I)

Unless indicated otherwise, in the following, R¹, R², R³, R⁴, R⁵ and R⁶have the same meaning as given above for compounds of formula (I).

The present invention relates to intermediates for the preparation ofcompounds of formula (I).

Compounds of formula (IVa) are provided:

whereinR¹ and R² are identical and are a chlorine atom or a bromine atom;R³ is methyl;U^(1a) is a hydroxy group or a C₁-C₆-alkoxy group,provided that the compound of formula (IVa) does not represent:

-   -   ethyl 4,5-dibromo-3-methylthiophene-2-carboxylate        [2088257-63-8],    -   4,5-dichloro-3-methylthiophene-2-carboxylic acid [854626-34-9],    -   4,5-dibromo-3-methylthiophene-2-carboxylic acid [854626-32-7],    -   methyl 4,5-dichloro-3-methylthiophene-2-carboxylate        [854626-27-0] and    -   methyl 4,5-dibromo-3-methylthiophene-2-carboxylate        [648412-53-7].

Compounds of formula (Via) are provided:

whereinR¹ and R² are identical and are a chlorine atom or a bromine atom;R⁴ is selected from the group consisting of hydrogen atom, C₁-C₆-alkyl,aralkyl, aralkyl substituted by hydroxyl, C₁-C₆-alkyl substituted by aC₁-C₆-alkylsulfanyl and R⁵ is a hydrogen atom; orR⁴ and R⁵ form, together with the carbon atom to which they are linked,a cyclopropyl;R⁶ is selected from the group consisting of hydrogen atom, C₁-C₆-alkyl,C₁-C₆-haloalkyl, C₁-C₆-cyanoalkyl, C₂-C₆-alkenyl, C₂-C₆-alkynyl,C₃-C₈-cycloalkyl, aryl, aralkyl, 4-, 5- or 6-membered heterocyclyl,—C₁-C₆-alkyl-Si(C₁-C₆-alkyl)₃ and —C₁-C₆-alkyl-C₃-C₈-cycloalkyl;U² _(a) is a bromine atom, an iodine atom, a mesylate group, a tosylategroup or a triflate group, wherein R⁴ is selected from the groupconsisting of hydrogen atom, C₁-C₆-alkyl, aralkyl, aralkyl substitutedby hydroxyl, C₁-C₆-alkyl substituted by a C₁-C₆-alkylsulfanyl and R⁵ isa hydrogen atom when R⁶ is hydrogen atom or C₁-C₆-alkyl; andprovided that when R¹ and R² are bromine atoms, U² _(a) is not a bromineatom.

Compounds of formula (VI)a wherein U² _(a) is a bromine atom or iodineatom have been found to be efficient in controlling fungi and/orbacteria.

Compounds of formula (Villa) are provided:

whereinR¹ and R² are identical and are a chlorine atom or a bromine atom;U^(1a) is a hydroxy group or a C₁-C₆-alkoxy group;U^(2a) is a bromine atom, an iodine atom, a mesylate group, a tosylategroup or a triflate group, provided that when R¹ and R² are bromineatoms, U^(2a) is not a bromine atom; andprovided that the compound of formula (Villa) does not represent:

-   -   methyl 4,5-dibromo-3-chlorothiophene-2-carboxylate        [1501789-47-4],    -   4,5-dibromo-3-iodothiophene-2-carboxylic acid [854626-46-3],    -   4,5-dibromo-3-chlorothiophene-2-carboxylic acid [503308-99-4]        and    -   ethyl 4,5-dibromo-3-chlorothiophene-2-carboxylate [503308-98-3].

Compounds of formula (Villa) are provided:

whereinR¹ and R² are identical and are a chlorine atom or a bromine atom;U^(1a) is a hydroxy group or a C₁-C₆-alkoxy group;U^(2a) is a mesylate group, a tosylate group or a triflate group.

Compounds of formula (Ixa) and (Ixb) are provided:

whereinR³ is methyl;R⁴ is selected from the group consisting of hydrogen atom, C₁-C₆-alkyl,aralkyl, aralkyl substituted by hydroxyl, C₁-C₆-alkyl substituted by aC₁-C₆-alkylsulfanyl and R⁵ is a hydrogen atom; orR⁴ and R⁵ form, together with the carbon atom to which they are linked,a cyclopropyl;R⁶ is selected from the group consisting of hydrogen atom, C₁-C₆-alkyl,C₁-C₆-haloalkyl, C₁-C₆-cyanoalkyl, C₂-C₆-alkenyl, C₂-C₆-alkynyl,C₃-C₈-cycloalkyl, aryl, aralkyl, 4-, 5- or 6-membered heterocyclyl,—C₁-C₆-alkyl-Si(C₁-C₆-alkyl)₃ and —C₁-C₆-alkyl-C₃-C₈-cycloalkyl;U^(4a) is a chlorine atom or a bromine atom; andU⁵ is a chlorine atom or a bromine atom.

Compounds of formula (Xa) and (Xb) are provided:

R¹ or R² is a chlorine atom or a bromine atom;R³ is methyl;R⁴ is selected from the group consisting of hydrogen atom, C₁-C₆-alkyl,aralkyl, aralkyl substituted by hydroxyl, C₁-C₆-alkyl substituted by aC₁-C₆-alkylsulfanyl and R⁵ is a hydrogen atom; orR⁴ and R⁵ form, together with the carbon atom to which they are linked,a cyclopropyl;R⁶ is selected from the group consisting of hydrogen atom, C₁-C₆-alkyl,C₁-C₆-haloalkyl, C₁-C₆-cyanoalkyl, C₂-C₆-alkenyl, C₂-C₆-alkynyl,C₃-C₈-cycloalkyl, aryl, aralkyl, 4-, 5- or 6-membered heterocyclyl,—C₁-C₆-alkyl-Si(C₁-C₆-alkyl)₃ and —C₁-C₆-alkyl-C₃-C₈-cycloalkyl;wherein R⁴ is selected from the group consisting of hydrogen atom,C₁-C₆-alkyl, aralkyl, aralkyl substituted by hydroxyl, C₁-C₆-alkylsubstituted by a C₁-C₆-alkylsulfanyl and R⁵ is a hydrogen atom when R⁶is hydrogen atom or C₁-C₆-alkyl.

Compounds of formula (XIa) and (XIb) are provided:

whereinR¹ or R² is a chlorine atom or a bromine atom;R³ is methyl;R⁴ is selected from the group consisting of hydrogen atom, C₁-C₆-alkyl,aralkyl, aralkyl substituted by hydroxyl, C₁-C₆-alkyl substituted by aC₁-C₆-alkylsulfanyl and R⁵ is a hydrogen atom; orR⁴ and R⁵ form, together with the carbon atom to which they are linked,a cyclopropyl;R⁶ is selected from the group consisting of hydrogen atom, C₁-C₆-alkyl,C₁-C₆-haloalkyl, C₁-C₆-cyanoalkyl, C₂-C₆-alkenyl, C₂-C₆-alkynyl,C₃-C₈-cycloalkyl, aryl, aralkyl, 4-, 5- or 6-membered heterocyclyl,—C₁-C₆-alkyl-Si(C₁-C₆-alkyl)₃ and —C₁-C₆-alkyl-C₃-C₈-cycloalkyl;V is a benzyl group, a 4-methoxybenzyl group, an allyl group, anunsubstituted or substituted C₁-C₆-alkoxycarbonyl, an unsubstituted orsubstituted benzyloxycarbonyl, an allyloxycarbonyl, an acetyl group or atrifluoroacetyl group;wherein R⁴ is selected from the group consisting of hydrogen atom,C₁-C₆-alkyl, aralkyl, aralkyl substituted by hydroxyl, C₁-C₆-alkylsubstituted by a C₁-C₆-alkylsulfanyl and R⁵ is a hydrogen atom when R⁶is hydrogen atom or C₁-C₆-alkyl.

Compounds of formula (XIIa) and (XIIb) are provided:

whereinR¹ or R² is a chlorine atom or a bromine atom;R³ is methyl;U^(1a) is a hydroxy group or a C₁-C₆-alkoxy group.provided that the compound of formula (XIIa) does not represent:

-   -   ethyl 5-amino-4-bromo-3-methylthiophene-2-carboxylate        [851443-15-7].

Compounds of formula (XIIIa) and (XIIIb) are provided:

whereinR¹ or R² is a chlorine atom or a bromine atom;R³ is methyl;V is a benzyl group, a 4-methoxybenzyl group, an allyl group, anunsubstituted or substituted C₁-C₆-alkoxycarbonyl, an unsubstituted orsubstituted benzyloxycarbonyl, an allyloxycarbonyl, an acetyl group or atrifluoroacetyl group; andU^(1a) is a hydroxy group or a C₁-C₆-alkoxy group,provided that the compound of formula (XIIIa) does not represent:

-   -   ethyl 5-acetamido-4-bromo-3-methylthiophene-2-carboxylate        [851444-63-8].

The disclosed intermediates may be efficient in controlling bacteriaand/or fungi.

Compositions and Formulations

The present invention further relates to a composition, in particular acomposition for controlling plant diseases caused by bacteria of thegenus Xanthomonas comprising one or more compounds of formula (I) asdisclosed herein above and any mixtures thereof.

The composition typically comprises at least one compound of formula (I)and at least one agriculturally suitable auxiliary, e.g. carrier(s)and/or surfactant(s).

A carrier is a solid or liquid, natural or synthetic, organic orinorganic substance that is generally inert. The carrier generallyimproves the application of the compounds, for instance, to plants,plants parts or seeds. Examples of suitable solid carriers include, butare not limited to, ammonium salts, natural rock flours, such askaolins, clays, talc, chalk, quartz, attapulgite, montmorillonite anddiatomaceous earth, and synthetic rock flours, such as finely dividedsilica, alumina and silicates. Examples of typically useful solidcarriers for preparing granules include, but are not limited to crushedand fractionated natural rocks such as calcite, marble, pumice,sepiolite and dolomite, synthetic granules of inorganic and organicflours and granules of organic material such as paper, sawdust, coconutshells, maize cobs and tobacco stalks. Examples of suitable liquidcarriers include, but are not limited to, water, organic solvents andcombinations thereof. Examples of suitable solvents include polar andnonpolar organic chemical liquids, for example from the classes ofaromatic and nonaromatic hydrocarbons (such as cyclohexane, paraffins,alkylbenzenes, xylene, toluene alkylnaphthalenes, chlorinated aromaticsor chlorinated aliphatic hydrocarbons such as chlorobenzenes,chloroethylenes or methylene chloride), alcohols and polyols (which mayoptionally also be substituted, etherified and/or esterified, such asbutanol or glycol), ketones (such as acetone, methyl ethyl ketone,methyl isobutyl ketone or cyclohexanone), esters (including fats andoils) and (poly)ethers, unsubstituted and substituted amines, amides(such as dimethylformamide), lactams (such as N-alkylpyrrolidones) andlactones, sulfones and sulfoxides (such as dimethyl sulfoxide). Thecarrier may also be a liquefied gaseous extender, i.e. liquid which isgaseous at standard temperature and under standard pressure, for exampleaerosol propellants such as halohydrocarbons, butane, propane, nitrogenand carbon dioxide. The amount of carrier typically ranges from 1 to99.99%, preferably from 5 to 99.9%, more preferably from 10 to 99.5%,and most preferably from 20 to 99% by weight of the composition.

The surfactant can be an ionic (cationic or anionic) or non-ionicsurfactant, such as ionic or non-ionic emulsifier(s), foam former(s),dispersant(s), wetting agent(s) and any mixtures thereof. Examples ofsuitable surfactants include, but are not limited to, salts ofpolyacrylic acid, salts of lignosulfonic acid, salts of phenolsulfonicacid or naphthalenesulfonic acid, polycondensates of ethylene and/orpropylene oxide with fatty alcohols, fatty acids or fatty amines(polyoxyethylene fatty acid esters, polyoxyethylene fatty alcoholethers, for example alkylaryl polyglycol ethers), substituted phenols(preferably alkylphenols or arylphenols), salts of sulfosuccinic esters,taurine derivatives (preferably alkyl taurates), phosphoric esters ofpolyethoxylated alcohols or phenols, fatty esters of polyols andderivatives of compounds containing sulfates, sulfonates, phosphates(for example, alkylsulfonates, alkyl sulfates, arylsulfonates) andprotein hydrolysates, lignosulfite waste liquors and methylcellulose. Asurfactant is typically used when the compounds of the invention and/orthe carrier are insoluble in water and the application is made withwater. Then, the amount of surfactants typically ranges from 5 to 40% byweight of the composition.

Further examples of suitable auxiliaries include water repellents,siccatives, binders (adhesive, tackifier, fixing agent, such ascarboxymethylcellulose, natural and synthetic polymers in the form ofpowders, granules or latices, such as gum arabic, polyvinyl alcohol andpolyvinyl acetate, natural phospholipids such as cephalins and lecithinsand synthetic phospholipids, polyvinylpyrrolidone and tylose),thickeners, stabilizers (e.g. cold stabilizers, preservatives,antioxidants, light stabilizers, or other agents which improve chemicaland/or physical stability), dyes or pigments (such as inorganicpigments, e.g. iron oxide, titanium oxide and Prussian Blue; organicdyes, e.g. alizarin, azo and metal phthalocyanine dyes), antifoams (e.g.silicone antifoams and magnesium stearate), preservatives (e.g.dichlorophene and benzyl alcohol hemiformal), secondary thickeners(cellulose derivatives, acrylic acid derivatives, xanthan, modifiedclays and finely divided silica), stickers, gibberellins and processingauxiliaries, mineral and vegetable oils, perfumes, waxes, nutrients(including trace nutrients, such as salts of iron, manganese, boron,copper, cobalt, molybdenum and zinc), protective colloids, thixotropicsubstances, penetrants, sequestering agents and complex formers.

The choice of the auxiliaries is related to the intended mode ofapplication of the compound of the invention and/or on the physicalproperties. Furthermore, the auxiliaries may be chosen to impartparticular properties (technical, physical and/or biological properties)to the compositions or use forms prepared therefrom. The choice ofauxiliaries may allow customizing the compositions to specific needs.

The composition of the invention may be in any customary form, such assolutions (e.g. aqueous solutions), emulsions, wettable powders, water-and oil-based suspensions, powders, dusts, pastes, soluble powders,soluble granules, granules for broadcasting, suspoemulsion concentrates,natural or synthetic products impregnated with the compound(s) of theinvention, fertilizers and also microencapsulations in polymericsubstances. The compound(s) of the invention may be present in asuspended, emulsified or dissolved form.

The composition of the invention may be provided to the end user asready-for-use formulation, i.e. the compositions may be directly appliedto the plants or seeds by a suitable device, such as a spraying ordusting device. Alternatively, the compositions may be provided to theend user in the form of concentrates which have to be diluted,preferably with water, prior to use.

The composition of the invention can be prepared in conventionalmanners, for example by mixing the compound(s) of the invention with oneor more suitable auxiliaries, such as disclosed herein above.

The composition according to the invention contains generally from 0.01to 99% by weight, from 0.05 to 98% by weight, preferably from 0.1 to 95%by weight, more preferably from 0.5 to 90% by weight, most preferablyfrom 1 to 80% by weight of the compound(s) of the invention. It ispossible that a composition comprises two or more compounds of theinvention. In such case the outlined ranges refer to the total amount ofcompounds of the present invention.

Mixtures/Combinations

The compound(s) and the composition of the invention can be mixed withother active ingredients like fungicides, bactericides, acaricides,nematicides, insecticides, herbicides, fertilizers, growth regulators,safeners and/or semiochemicals. This may allow to broaden the activityspectrum or to prevent development of resistance. Examples of knownfungicides, insecticides, acaricides, nematicides and bactericides aredisclosed in the Pesticide Manual, 17^(th) Edition.

Examples of especially preferred fungicides which could be mixed withthe compound(s) and the composition of the invention are:

1) Inhibitors of the ergosterol biosynthesis, for example (1.001)cyproconazole, (1.002) difenoconazole, (1.003) epoxiconazole, (1.004)fenhexamid, (1.005) fenpropidin, (1.006) fenpropimorph, (1.007)fenpyrazamine, (1.008) fluquinconazole, (1.009) flutriafol, (1.010)imazalil, (1.011) imazalil sulfate, (1.012) ipconazole, (1.013)metconazole, (1.014) myclobutanil, (1.015) paclobutrazol, (1.016)prochloraz, (1.017) propiconazole, (1.018) prothioconazole, (1.019)pyrisoxazole, (1.020) spiroxamine, (1.021) tebuconazole, (1.022)tetraconazole, (1.023) triadimenol, (1.024) tridemorph, (1.025)triticonazole, (1.026)(1R,2S,5S)-5-(4-chlorobenzyl)-2-(chloromethyl)-2-methyl-1-(1H-1,2,4-triazol-1-ylmethyl)cyclopentanol,(1.027)(1S,2R,5R)-5-(4-chlorobenzyl)-2-(chloromethyl)-2-methyl-1-(1H-1,2,4-triazol-1-ylmethyl)cyclopentanol,(1.028)(2R)-2-(1-chlorocyclopropyl)-4-[(1R)-2,2-dichlorocyclopropyl]-1-(1H-1,2,4-triazol-1-yl)butan-2-ol,(1.029) (2R)-2-(1-chlorocyclopropyl)-4-[(1S)-2,2-dichlorocyclopropyl]-1-(1H-1,2,4-triazol-1-yl)butan-2-ol, (1.030)(2R)-2-[4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl]-1-(1H-1,2,4-triazol-1-yl)propan-2-ol,(1.031)(2S)-2-(1-chlorocyclopropyl)-4-[(1R)-2,2-dichlorocyclopropyl]-1-(1H-1,2,4-triazol-1-yl)butan-2-ol,(1.032) (2S)-2-(1-chlorocyclopropyl)-4-[(1S)-2,2-dichlorocyclopropyl]-1-(1H-1,2,4-triazol-1-yl)butan-2-ol, (1.033)(2S)-2-[4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl]-1-(1H-1,2,4-triazol-1-yl)propan-2-ol,(1.034)(R)-[3-(4-chloro-2-fluorophenyl)-5-(2,4-difluorophenyl)-1,2-oxazol-4-yl](pyridin-3-yl)methanol,(1.035)(S)-[3-(4-chloro-2-fluorophenyl)-5-(2,4-difluorophenyl)-1,2-oxazol-4-yl](pyridin-3-yl)methanol,(1.036)[3-(4-chloro-2-fluorophenyl)-5-(2,4-difluorophenyl)-1,2-oxazol-4-yl](pyridin-3-yl)methanol,(1.037)1-({(2R,4S)-2-[2-chloro-4-(4-chlorophenoxy)phenyl]-4-methyl-1,3-dioxolan-2-yl}methyl)-1H-1,2,4-triazole,(1.038)1-({(2S,4S)-2-[2-chloro-4-(4-chlorophenoxy)phenyl]-4-methyl-1,3-dioxolan-2-yl}methyl)-1H-1,2,4-triazole,(1.039)1-{[3-(2-chlorophenyl)-2-(2,4-difluorophenyl)oxiran-2-yl]methyl}-1H-1,2,4-triazol-5-ylthiocyanate, (1.040)1-{[rel(2R,3R)-3-(2-chlorophenyl)-2-(2,4-difluorophenyl)oxiran-2-yl]methyl}-1H-1,2,4-triazol-5-ylthiocyanate, (1.041)1-{[rel(2R,3S)-3-(2-chlorophenyl)-2-(2,4-difluorophenyl)oxiran-2-yl]methyl}-1H-1,2,4-triazol-5-ylthiocyanate, (1.042)2-[(2R,4R,5R)-1-(2,4-dichlorophenyl)-5-hydroxy-2,6,6-trimethylheptan-4-yl]-2,4-dihydro-3H-1,2,4-triazole-3-thione,(1.043)2-[(2R,4R,5S)-1-(2,4-dichlorophenyl)-5-hydroxy-2,6,6-trimethylheptan-4-yl]-2,4-dihydro-3H-1,2,4-triazole-3-thione,(1.044)2-[(2R,4S,5R)-1-(2,4-dichlorophenyl)-5-hydroxy-2,6,6-trimethylheptan-4-yl]-2,4-dihydro-3H-1,2,4-triazole-3-thione,(1.045)2-[(2R,4S,5S)-1-(2,4-dichlorophenyl)-5-hydroxy-2,6,6-trimethylheptan-4-yl]-2,4-dihydro-3H-1,2,4-triazole-3-thione,(1.046)2-[(2S,4R,5R)-1-(2,4-dichlorophenyl)-5-hydroxy-2,6,6-trimethylheptan-4-yl]-2,4-dihydro-3H-1,2,4-triazole-3-thione,(1.047)2-[(2S,4R,5S)-1-(2,4-dichlorophenyl)-5-hydroxy-2,6,6-trimethylheptan-4-yl]-2,4-dihydro-3H-1,2,4-triazole-3-thione,(1.048)2-[(2S,4S,5R)-1-(2,4-dichlorophenyl)-5-hydroxy-2,6,6-trimethylheptan-4-yl]-2,4-dihydro-3H-1,2,4-triazole-3-thione,(1.049)2-[(2S,4S,5S)-1-(2,4-dichlorophenyl)-5-hydroxy-2,6,6-trimethylheptan-4-yl]-2,4-dihydro-3H-1,2,4-triazole-3-thione,(1.050)2-[1-(2,4-dichlorophenyl)-5-hydroxy-2,6,6-trimethylheptan-4-yl]-2,4-dihydro-3H-1,2,4-triazole-3-thione,(1.051)2-[2-chloro-4-(2,4-dichlorophenoxy)phenyl]-1-(1H-1,2,4-triazol-1-yl)propan-2-ol,(1.052)2-[2-chloro-4-(4-chlorophenoxy)phenyl]-1-(1H-1,2,4-triazol-1-yl)butan-2-ol,(1.053)2-[4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl]-1-(1H-1,2,4-triazol-1-yl)butan-2-ol,(1.054)2-[4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl]-1-(1H-1,2,4-triazol-1-yl)pentan-2-ol,(1.055) Mefentrifluconazole, (1.056)2-{[3-(2-chlorophenyl)-2-(2,4-difluorophenyl)oxiran-2-yl]methyl}-2,4-dihydro-3H-1,2,4-triazole-3-thione,(1.057)2-{[rel(2R,3R)-3-(2-chlorophenyl)-2-(2,4-difluorophenyl)oxiran-2-yl]methyl}-2,4-dihydro-3H-1,2,4-triazole-3-thione,(1.058)2-{[rel(2R,3S)-3-(2-chlorophenyl)-2-(2,4-difluorophenyl)oxiran-2-yl]methyl}-2,4-dihydro-3H-1,2,4-triazole-3-thione,(1.059)5-(4-chlorobenzyl)-2-(chloromethyl)-2-methyl-1-(1H-1,2,4-triazol-1-ylmethyl)cyclopentanol,(1.060)5-(allylsulfanyl)-1-{[3-(2-chlorophenyl)-2-(2,4-difluorophenyl)oxiran-2-yl]methyl}-1H-1,2,4-triazole,(1.061)5-(allylsulfanyl)-1-{[rel(2R,3R)-3-(2-chlorophenyl)-2-(2,4-difluorophenyl)oxiran-2-yl]methyl}-1H-1,2,4-triazole,(1.062)5-(allylsulfanyl)-1-{[rel(2R,3S)-3-(2-chlorophenyl)-2-(2,4-difluorophenyl)oxiran-2-yl]methyl}-1H-1,2,4-triazole,(1.063)N′-(2,5-dimethyl-4-{[3-(1,1,2,2-tetrafluoroethoxy)phenyl]sulfanyl}phenyl)-N-ethyl-N-methylimidoformamide,(1.064)N′-(2,5-dimethyl-4-{[3-(2,2,2-trifluoroethoxy)phenyl]sulfanyl}phenyl)-N-ethyl-N-methylimidoformamide,(1.065)N′-(2,5-dimethyl-4-{[3-(2,2,3,3-tetrafluoropropoxy)phenyl]sulfanyl}phenyl)-N-ethyl-N-methylimidoformamide,(1.066)N′-(2,5-dimethyl-4-{[3-(pentafluoroethoxy)phenyl]sulfanyl}phenyl)-N-ethyl-N-methylimidoformamide,(1.067)N′-(2,5-dimethyl-4-{3-[(1,1,2,2-tetrafluoroethyl)sulfanyl]phenoxy}phenyl)-N-ethyl-N-methylimidoformamide,(1.068)N′-(2,5-dimethyl-4-{3-[(2,2,2-trifluoroethyl)sulfanyl]phenoxy}phenyl)-N-ethyl-N-methylimido-formamide,(1.069)N′-(2,5-dimethyl-4-{3-[(2,2,3,3-tetrafluoropropyl)sulfanyl]phenoxy}phenyl)-N-ethyl-N-methylimidoformamide,(1.070)N′-(2,5-dimethyl-4-{3-[(pentafluoroethyl)sulfanyl]phenoxy}phenyl)-N-ethyl-N-methylimidoformamide,(1.071)N′-(2,5-dimethyl-4-phenoxyphenyl)-N-ethyl-N-methylimidoformamide,(1.072)N′-(4-{[3-(difluoromethoxy)phenyl]sulfanyl}-2,5-dimethylphenyl)-N-ethyl-N-methylimidoformamide,(1.073)N′-(4-{3-[(difluoromethyl)sulfanyl]phenoxy}-2,5-dimethylphenyl)-N-ethyl-N-methylimidoformamide,(1.074)N′-[5-bromo-6-(2,3-dihydro-1H-inden-2-yloxy)-2-methylpyridin-3-yl]-N-ethyl-N-methylimidoformamide,(1.075)N′-{4-[(4,5-dichloro-1,3-thiazol-2-yl)oxy]-2,5-dimethylphenyl}-N-ethyl-N-methylimidoformamide,(1.076)N′-{5-bromo-6-[(1R)-1-(3,5-difluorophenyl)ethoxy]-2-methylpyridin-3-yl}-N-ethyl-N-methylimidoformamide,(1.077) N′-{5-bromo-6-[(1S)-1-(3,5-difluorophenyl)ethoxy]-2-methylpyridin-3-yl}-N-ethyl-N-methylimidoformamide,(1.078)N′-{5-bromo-6-[(cis-4-isopropylcyclohexyl)oxy]-2-methylpyridin-3-yl}-N-ethyl-N-methylimidoformamide,(1.079)N′-{5-bromo-6-[(trans-4-isopropylcyclohexyl)oxy]-2-methylpyridin-3-yl}-N-ethyl-N-methylimidoformamide,(1.080)N′-{5-bromo-6-[1-(3,5-difluorophenyl)ethoxy]-2-methylpyridin-3-yl}-N-ethyl-N-methylimidoformamide,(1.081) Ipfentrifluconazole.2) Inhibitors of the respiratory chain at complex I or II, for example(2.001) benzovindiflupyr, (2.002) bixafen, (2.003) boscalid, (2.004)carboxin, (2.005) fluopyram, (2.006) flutolanil, (2.007) fluxapyroxad,(2.008) furametpyr, (2.009) Isofetamid, (2.010) isopyrazam(anti-epimeric enantiomer 1R,4S,9S), (2.011) isopyrazam (anti-epimericenantiomer 1S,4R,9R), (2.012) isopyrazam (anti-epimeric racemate1RS,4SR,9SR), (2.013) isopyrazam (mixture of syn-epimeric racemate1RS,4SR,9RS and anti-epimeric racemate 1RS,4SR,9SR), (2.014) isopyrazam(syn-epimeric enantiomer 1R,4S,9R), (2.015) isopyrazam (syn-epimericenantiomer 1S,4R,9S), (2.016) isopyrazam (syn-epimeric racemate1RS,4SR,9RS), (2.017) penflufen, (2.018) penthiopyrad, (2.019)pydiflumetofen, (2.020) pyraziflumid, (2.021) sedaxane, (2.022)1,3-dimethyl-N-(1,1,3-trimethyl-2,3-dihydro-1H-inden-4-yl)-1H-pyrazole-4-carboxamide,(2.023)1,3-dimethyl-N-[(3R)-1,1,3-trimethyl-2,3-dihydro-1H-inden-4-yl]-1H-pyrazole-4-carboxamide,(2.024)1,3-dimethyl-N-[(3S)-1,1,3-trimethyl-2,3-dihydro-1H-inden-4-yl]-1H-pyrazole-4-carboxamide,(2.025)1-methyl-3-(trifluoromethyl)-N-[2′-(trifluoromethyl)biphenyl-2-yl]-1H-pyrazole-4-carboxamide,(2.026)2-fluoro-6-(trifluoromethyl)-N-(1,1,3-trimethyl-2,3-dihydro-1H-inden-4-yl)benzamide,(2.027)3-(difluoromethyl)-1-methyl-N-(1,1,3-trimethyl-2,3-dihydro-1H-inden-4-yl)-1H-pyrazole-4-carboxamide,(2.028)3-(difluoromethyl)-1-methyl-N-[(3R)-1,1,3-trimethyl-2,3-dihydro-1H-inden-4-yl]-1H-pyrazole-4-carboxamide,(2.029)3-(difluoromethyl)-1-methyl-N-[(3S)-1,1,3-trimethyl-2,3-dihydro-1H-inden-4-yl]-1H-pyrazole-4-carboxamide,(2.030) fluindapyr, (2.031)3-(difluoromethyl)-N-[(3R)-7-fluoro-1,1,3-trimethyl-2,3-dihydro-1H-inden-4-yl]-1-methyl-1H-pyrazole-4-carboxamide,(2.032)3-(difluoromethyl)-N-[(3S)-7-fluoro-1,1,3-trimethyl-2,3-dihydro-1H-inden-4-yl]-1-methyl-1H-pyrazole-4-carboxamide,(2.033)5,8-difluoro-N-[2-(2-fluoro-4-{[4-(trifluoromethyl)pyridin-2-yl]oxy}-phenyl)ethyl]quinazolin-4-amine,(2.034)N-(2-cyclopentyl-5-fluorobenzyl)-N-cyclopropyl-3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxamide,(2.035)N-(2-tert-butyl-5-methylbenzyl)-N-cyclopropyl-3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxamide,(2.036)N-(2-tert-butylbenzyl)-N-cyclopropyl-3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxamide,(2.037)N-(5-chloro-2-ethylbenzyl)-N-cyclopropyl-3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxamide,(2.038) isoflucypram, (2.039)N-[(1R,4S)-9-(dichloromethylene)-1,2,3,4-tetrahydro-1,4-methanonaphthalen-5-yl]-3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxamide,(2.040)N-[(1S,4R)-9-(dichloromethylene)-1,2,3,4-tetrahydro-1,4-methanonaphthalen-5-yl]-3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxamide,(2.041)N-[1-(2,4-dichlorophenyl)-1-methoxypropan-2-yl]-3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxamide,(2.042)N-[2-chloro-6-(trifluoromethyl)benzyl]-N-cyclopropyl-3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxamide,(2.043)N-[3-chloro-2-fluoro-6-(trifluoromethyl)benzyl]-N-cyclopropyl-3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxamide,(2.044)N-[5-chloro-2-(trifluoromethyl)benzyl]-N-cyclopropyl-3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxamide,(2.045)N-cyclopropyl-3-(difluoromethyl)-5-fluoro-1-methyl-N-[5-methyl-2-(trifluoromethyl)benzyl]-1H-pyrazole-4-carboxamide,(2.046)N-cyclopropyl-3-(difluoromethyl)-5-fluoro-N-(2-fluoro-6-isopropylbenzyl)-1-methyl-1H-pyrazole-4-carboxamide,(2.047)N-cyclopropyl-3-(difluoromethyl)-5-fluoro-N-(2-isopropyl-5-methylbenzyl)-1-methyl-1H-pyrazole-4-carboxamide,(2.048)N-cyclopropyl-3-(difluoromethyl)-5-fluoro-N-(2-isopropylbenzyl)-1-methyl-1H-pyrazole-4-carbothioamide,(2.049)N-cyclopropyl-3-(difluoromethyl)-5-fluoro-N-(2-isopropylbenzyl)-1-methyl-1H-pyrazole-4-carboxamide,(2.050)N-cyclopropyl-3-(difluoromethyl)-5-fluoro-N-(5-fluoro-2-isopropylbenzyl)-1-methyl-1H-pyrazole-4-carboxamide,(2.051)N-cyclopropyl-3-(difluoromethyl)-N-(2-ethyl-4,5-dimethylbenzyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxamide,(2.052)N-cyclopropyl-3-(difluoromethyl)-N-(2-ethyl-5-fluorobenzyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxamide,(2.053)N-cyclopropyl-3-(difluoromethyl)-N-(2-ethyl-5-methylbenzyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxamide,(2.054)N-cyclopropyl-N-(2-cyclopropyl-5-fluorobenzyl)-3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxamide,(2.055)N-cyclopropyl-N-(2-cyclopropyl-5-methylbenzyl)-3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxamide,(2.056)N-cyclopropyl-N-(2-cyclopropylbenzyl)-3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxamide,(2.057) pyrapropoyne.3) Inhibitors of the respiratory chain at complex III, for example(3.001) ametoctradin, (3.002) amisulbrom, (3.003) azoxystrobin, (3.004)coumethoxystrobin, (3.005) coumoxystrobin, (3.006) cyazofamid, (3.007)dimoxystrobin, (3.008) enoxastrobin, (3.009) famoxadone, (3.010)fenamidone, (3.011) flufenoxystrobin, (3.012) fluoxastrobin, (3.013)kresoxim-methyl, (3.014) metominostrobin, (3.015) orysastrobin, (3.016)picoxystrobin, (3.017) pyraclostrobin, (3.018) pyrametostrobin, (3.019)pyraoxystrobin, (3.020) trifloxystrobin, (3.021)(2E)-2-{2-[({[(1E)-1-(3-{[(E)-1-fluoro-2-phenylvinyl]oxy}phenyl)ethylidene]amino}oxy)methyl]phenyl}-2-(methoxyimino)-N-methylacetamide,(3.022)(2E,3Z)-5-{[1-(4-chlorophenyl)-1H-pyrazol-3-yl]oxy}-2-(methoxyimino)-N,3-dimethylpent-3-enamide,(3.023)(2R)-2-{2-[(2,5-dimethylphenoxy)methyl]phenyl}-2-methoxy-N-methylacetamide,(3.024)(2S)-2-{2-[(2,5-dimethylphenoxy)methyl]phenyl}-2-methoxy-N-methylacetamide,(3.025)(3S,6S,7R,8R)-8-benzyl-3-[({3-[(isobutyryloxy)methoxy]-4-methoxypyridin-2-yl}carbonyl)amino]-6-methyl-4,9-dioxo-1,5-dioxonan-7-yl2-methylpropanoate, (3.026) mandestrobin, (3.027)N-(3-ethyl-3,5,5-trimethylcyclohexyl)-3-formamido-2-hydroxybenzamide,(3.028)(2E,3Z)-5-{[1-(4-chloro-2-fluorophenyl)-1H-pyrazol-3-yl]oxy}-2-(methoxyimino)-N,3-dimethylpent-3-enamide,(3.029) methyl{5-[3-(2,4-dimethylphenyl)-1H-pyrazol-1-yl]-2-methylbenzyl}carbamate,(3.030) metyltetraprole, (3.031) florylpicoxamid.4) Inhibitors of the mitosis and cell division, for example (4.001)carbendazim, (4.002) diethofencarb, (4.003) ethaboxam, (4.004)fluopicolide, (4.005) pencycuron, (4.006) thiabendazole, (4.007)thiophanate-methyl, (4.008) zoxamide, (4.009)3-chloro-4-(2,6-difluorophenyl)-6-methyl-5-phenylpyridazine, (4.010)3-chloro-5-(4-chlorophenyl)-4-(2,6-difluorophenyl)-6-methylpyridazine,(4.011)3-chloro-5-(6-chloropyridin-3-yl)-6-methyl-4-(2,4,6-trifluorophenyl)pyridazine,(4.012)4-(2-bromo-4-fluorophenyl)-N-(2,6-difluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine,(4.013)4-(2-bromo-4-fluorophenyl)-N-(2-bromo-6-fluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine,(4.014)4-(2-bromo-4-fluorophenyl)-N-(2-bromophenyl)-1,3-dimethyl-1H-pyrazol-5-amine,(4.015)4-(2-bromo-4-fluorophenyl)-N-(2-chloro-6-fluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine,(4.016)4-(2-bromo-4-fluorophenyl)-N-(2-chlorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine,(4.017)4-(2-bromo-4-fluorophenyl)-N-(2-fluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine,(4.018)4-(2-chloro-4-fluorophenyl)-N-(2,6-difluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine,(4.019)4-(2-chloro-4-fluorophenyl)-N-(2-chloro-6-fluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine,(4.020)4-(2-chloro-4-fluorophenyl)-N-(2-chlorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine,(4.021)4-(2-chloro-4-fluorophenyl)-N-(2-fluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine,(4.022)4-(4-chlorophenyl)-5-(2,6-difluorophenyl)-3,6-dimethylpyridazine,(4.023)N-(2-bromo-6-fluorophenyl)-4-(2-chloro-4-fluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine,(4.024)N-(2-bromophenyl)-4-(2-chloro-4-fluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine,(4.025)N-(4-chloro-2,6-difluorophenyl)-4-(2-chloro-4-fluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine.5) Compounds having a multisite action, for example (5.001) bordeauxmixture, (5.002) captafol, (5.003) captan, (5.004) chlorothalonil,(5.005) copper hydroxide, (5.006) copper naphthenate, (5.007) copperoxide, (5.008) copper oxychloride, (5.009) copper(2+) sulfate, (5.010)dithianon, (5.011) dodine, (5.012) folpet, (5.013) mancozeb, (5.014)maneb, (5.015) metiram, (5.016) metiram zinc, (5.017) oxine-copper,(5.018) propineb, (5.019) sulfur and sulfur preparations includingcalcium polysulfide, (5.020) thiram, (5.021) zineb, (5.022) ziram,(5.023)6-ethyl-5,7-dioxo-6,7-dihydro-5H-pyrrolo[3′,4′:5,6][1,4]dithiino[2,3-c][1,2]thiazole-3-carbonitrile.6) Compounds inducing a host defense, for example (6.001)acibenzolar-S-methyl, (6.002) isotianil, (6.003) probenazole, (6.004)tiadinil.7) Inhibitors of the amino acid and/or protein biosynthesis, for example(7.001) cyprodinil, (7.002) kasugamycin, (7.003) kasugamycinhydrochloride hydrate, (7.004) oxytetracycline, (7.005) pyrimethanil,(7.006)3-(5-fluoro-3,3,4,4-tetramethyl-3,4-dihydroisoquinolin-1-yl)quinoline.8) Inhibitors of the ATP production, for example (8.001) silthiofam.9) Inhibitors of the cell wall synthesis, for example (9.001)benthiavalicarb, (9.002) dimethomorph, (9.003) flumorph, (9.004)iprovalicarb, (9.005) mandipropamid, (9.006) pyrimorph, (9.007)valifenalate, (9.008)(2E)-3-(4-tert-butylphenyl)-3-(2-chloropyridin-4-yl)-1-(morpholin-4-yl)prop-2-en-1-one,(9.009)(2Z)-3-(4-tert-butylphenyl)-3-(2-chloropyridin-4-yl)-1-(morpholin-4-yl)prop-2-en-1-one.10) Inhibitors of the lipid and membrane synthesis, for example (10.001)propamocarb, (10.002) propamocarb hydrochloride, (10.003)tolclofos-methyl.11) Inhibitors of the melanin biosynthesis, for example (11.001)tricyclazole, (11.002) 2,2,2-trifluoroethyl{3-methyl-1-[(4-methylbenzoyl)amino]butan-2-yl}carbamate.12) Inhibitors of the nucleic acid synthesis, for example (12.001)benalaxyl, (12.002) benalaxyl-M (kiralaxyl), (12.003) metalaxyl,(12.004) metalaxyl-M (mefenoxam).13) Inhibitors of the signal transduction, for example (13.001)fludioxonil, (13.002) iprodione, (13.003) procymidone, (13.004)proquinazid, (13.005) quinoxyfen, (13.006) vinclozolin.14) Compounds acting as an uncoupler, for example (14.001) fluazinam,(14.002) meptyldinocap.15) Further compounds, for example (15.001) abscisic acid, (15.002)benthiazole, (15.003) bethoxazin, (15.004) capsimycin, (15.005) carvone,(15.006) chinomethionat, (15.007) cufraneb, (15.008) cyflufenamid,(15.009) cymoxanil, (15.010) cyprosulfamide, (15.011) flutianil,(15.012) fosetyl-aluminium, (15.013) fosetyl-calcium, (15.014)fosetyl-sodium, (15.015) methyl isothiocyanate, (15.016) metrafenone,(15.017) mildiomycin, (15.018) natamycin, (15.019) nickeldimethyldithiocarbamate, (15.020) nitrothal-isopropyl, (15.021)oxamocarb, (15.022) oxathiapiprolin, (15.023) oxyfenthiin, (15.024)pentachlorophenol and salts, (15.025) phosphorous acid and its salts,(15.026) propamocarb-fosetylate, (15.027) pyriofenone (chlazafenone),(15.028) tebufloquin, (15.029) tecloftalam, (15.030) tolnifanide,(15.031)1-(4-{4-[(5R)-5-(2,6-difluorophenyl)-4,5-dihydro-1,2-oxazol-3-yl]-1,3-thiazol-2-yl}piperidin-1-yl)-2-[5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]ethanone,(15.032)1-(4-{4-[(5S)-5-(2,6-difluorophenyl)-4,5-dihydro-1,2-oxazol-3-yl]-1,3-thiazol-2-yl}piperidin-1-yl)-2-[5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]ethanone,(15.033) 2-(6-benzylpyridin-2-yl)quinazoline, (15.034) dipymetitrone,(15.035)2-[3,5-bis(difluoromethyl)-1H-pyrazol-1-yl]-1-[4-(4-{5-[2-(prop-2-yn-1-yloxy)phenyl]-4,5-dihydro-1,2-oxazol-3-yl}-1,3-thiazol-2-yl)piperidin-1-yl]ethanone,(15.036)2-[3,5-bis(difluoromethyl)-1H-pyrazol-1-yl]-1-[4-(4-{5-[2-chloro-6-(prop-2-yn-1-yloxy)phenyl]-4,5-dihydro-1,2-oxazol-3-yl}-1,3-thiazol-2-yl)piperidin-1-yl]ethanone,(15.037)2-[3,5-bis(difluoromethyl)-1H-pyrazol-1-yl]-1-[4-(4-{5-[2-fluoro-6-(prop-2-yn-1-yloxy)phenyl]-4,5-dihydro-1,2-oxazol-3-yl}-1,3-thiazol-2-yl)piperidin-1-yl]ethanone,(15.038)2-[6-(3-fluoro-4-methoxyphenyl)-5-methylpyridin-2-yl]quinazoline,(15.039)2-{(5R)-3-[2-(1-{[3,5-bis(difluoromethyl)-1H-pyrazol-1-yl]acetyl}piperidin-4-yl)-1,3-thiazol-4-yl]-4,5-dihydro-1,2-oxazol-5-yl}-3-chlorophenylmethanesulfonate, (15.040)2-{(5S)-3-[2-(1-{[3,5-bis(difluoromethyl)-1H-pyrazol-1-yl]acetyl}piperidin-4-yl)-1,3-thiazol-4-yl]-4,5-dihydro-1,2-oxazol-5-yl}-3-chlorophenylmethanesulfonate, (15.041) Ipflufenoquin, (15.042)2-{2-fluoro-6-[(8-fluoro-2-methylquinolin-3-yl)oxy]phenyl}propan-2-ol,(15.043)2-{3-[2-(1-{[3,5-bis(difluoromethyl)-1H-pyrazol-1-yl]acetyl}piperidin-4-yl)-1,3-thiazol-4-yl]-4,5-dihydro-1,2-oxazol-5-yl}-3-chlorophenylmethanesulfonate, (15.044)2-{3-[2-(1-{[3,5-bis(difluoromethyl)-1H-pyrazol-1-yl]acetyl}piperidin-4-yl)-1,3-thiazol-4-yl]-4,5-dihydro-1,2-oxazol-5-yl}phenylmethanesulfonate, (15.045) 2-phenylphenol and salts, (15.046)3-(4,4,5-trifluoro-3,3-dimethyl-3,4-dihydroisoquinolin-1-yl)quinoline,(15.047) quinofumelin, (15.048) 4-amino-5-fluoropyrimidin-2-ol(tautomeric form: 4-amino-5-fluoropyrimidin-2(1H)-one), (15.049)4-oxo-4-[(2-phenylethyl)amino]butanoic acid, (15.050)5-amino-1,3,4-thiadiazole-2-thiol, (15.051)5-chloro-N′-phenyl-N′-(prop-2-yn-1-yl)thiophene-2-sulfonohydrazide,(15.052) 5-fluoro-2-[(4-fluorobenzyl)oxy]pyrimidin-4-amine, (15.053)5-fluoro-2-[(4-methylbenzyl)oxy]pyrimidin-4-amine, (15.054)9-fluoro-2,2-dimethyl-5-(quinolin-3-yl)-2,3-dihydro-1,4-benzoxazepine,(15.055) but-3-yn-1-yl{6-[({[(Z)-(1-methyl-1H-tetrazol-5-yl)(phenyl)methylene]amino}oxy)methyl]pyridin-2-yl}carbamate,(15.056) ethyl (2Z)-3-amino-2-cyano-3-phenylacrylate, (15.057)phenazine-1-carboxylic acid, (15.058) propyl 3,4,5-trihydroxybenzoate,(15.059) quinolin-8-ol, (15.060) quinolin-8-ol sulfate (2:1), (15.061)tert-butyl{6-[({[(1-methyl-1H-tetrazol-5-yl)(phenyl)methylene]amino}oxy)methyl]pyridin-2-yl}carbamate,(15.062)5-fluoro-4-imino-3-methyl-1-[(4-methylphenyl)sulfonyl]-3,4-dihydropyrimidin-2(1H)-one,(15.063) aminopyrifen.

All named mixing partners of the classes (1) to (15) as described hereabove can be present in the form of the free compound and/or, if theirfunctional groups enable this, an agriculturally acceptable saltthereof.

In some embodiments, the compound combinations comprise the followingcomponents:

(I.01)+(I.001), (I.01)+(I.002), (I.01)+(I.003), (I.01)+(I.004),(I.01)+(I.005), (I.01)+(I.006), (I.01)+(I.007), (I.01)+(I.008),(I.01)+(I.009), (I.01)+(I.010), (I.01)+(I.011), (I.01)+(I.012),(I.01)+(I.013), (I.01)+(I.014), (I.01)+(I.015), (I.01)+(I.016),(I.01)+(I.017), (I.01)+(I.018), (I.01)+(I.019), (I.01)+(I.020),(I.01)+(I.021), (I.01)+(I.022), (I.01)+(I.023), (I.01)+(I.024),(I.01)+(I.025), (I.01)+(I.026), (I.01)+(I.027), (I.01)+(I.028),(I.01)+(I.029), (I.01)+(I.030), (I.01)+(I.031), (I.01)+(I.032),(I.01)+(I.033), (I.01)+(I.034), (I.01)+(I.035), (I.01)+(I.036),(I.01)+(I.037), (I.01)+(I.038), (I.01)+(I.039), (I.01)+(I.040),(I.01)+(I.041), (I.01)+(I.042), (I.01)+(I.043), (I.01)+(I.044),(I.01)+(I.045), (I.01)+(I.046), (I.01)+(I.047), (I.01)+(I.048),(I.01)+(I.049), (I.01)+(I.050), (I.01)+(I.051), (I.01)+(I.052),(I.01)+(I.053), (I.01)+(I.054), (I.01)+(I.055), (I.01)+(I.056),(I.01)+(I.057), (I.01)+(I.058), (I.01)+(I.059), (I.01)+(I.060),(I.01)+(I.061), (I.01)+(I.062), (I.01)+(I.063), (I.01)+(I.064),(I.01)+(I.065), (I.01)+(I.066), (I.01)+(I.067), (I.01)+(I.068),(I.01)+(I.069), (I.01)+(I.070), (I.01)+(I.071), (I.01)+(I.072),(I.01)+(I.073), (I.01)+(I.074), (I.01)+(I.075), (I.01)+(I.076),(I.01)+(I.077), (I.01)+(I.078), (I.01)+(I.079), (I.01)+(I.080),(I.01)+(I.081), (I.01)+(I.082), (I.01)+(I.083), (I.01)+(I.084),(I.01)+(I.085), (I.01)+(I.086), (I.01)+(2.001), (I.01)+(2.002),(I.01)+(2.003), (I.01)+(2.004), (I.01)+(2.005), (I.01)+(2.006),(I.01)+(2.007), (I.01)+(2.008), (I.01)+(2.009), (I.01)+(2.010),(I.01)+(2.011), (I.01)+(2.012), (I.01)+(2.013), (I.01)+(2.014),(I.01)+(2.015), (I.01)+(2.016), (I.01)+(2.017), (I.01)+(2.018),(I.01)+(2.019), (I.01)+(2.020), (I.01)+(2.021), (I.01)+(2.022),(I.01)+(2.023), (I.01)+(2.024), (I.01)+(2.025), (I.01)+(2.026),(I.01)+(2.027), (I.01)+(2.028), (I.01)+(2.029), (I.01)+(2.030),(I.01)+(2.031), (I.01)+(2.032), (I.01)+(2.033), (I.01)+(2.034),(I.01)+(2.035), (I.01)+(2.036), (I.01)+(2.037), (I.01)+(2.038),(I.01)+(2.039), (I.01)+(2.040), (I.01)+(2.041), (I.01)+(2.042),(I.01)+(2.043), (I.01)+(2.044), (I.01)+(2.045), (I.01)+(2.046),(I.01)+(2.047), (I.01)+(2.048), (I.01)+(2.049), (I.01)+(2.050),(I.01)+(2.051), (I.01)+(2.052), (I.01)+(2.053), (I.01)+(2.054),(I.01)+(2.055), (I.01)+(2.056), (I.01)+(3.001), (I.01)+(3.002),(I.01)+(3.003), (I.01)+(3.004), (I.01)+(3.005), (I.01)+(3.006),(I.01)+(3.007), (I.01)+(3.008), (I.01)+(3.009), (I.01)+(3.010),(I.01)+(3.011), (I.01)+(3.012), (I.01)+(3.013), (I.01)+(3.014),(I.01)+(3.015), (I.01)+(3.016), (I.01)+(3.017), (I.01)+(3.018),(I.01)+(3.019), (I.01)+(3.020), (I.01)+(3.021), (I.01)+(3.022),(I.01)+(3.023), (I.01)+(3.024), (I.01)+(3.025), (I.01)+(3.026),(I.01)+(3.027), (I.01)+(3.028), (I.01)+(3.029), (I.01)+(3.030),(I.01)+(4.001), (I.01)+(4.002), (I.01)+(4.003), (I.01)+(4.004),(I.01)+(4.005), (I.01)+(4.006), (I.01)+(4.007), (I.01)+(4.008),(I.01)+(4.009), (I.01)+(4.010), (I.01)+(4.011), (I.01)+(4.012),(I.01)+(4.013), (I.01)+(4.014), (I.01)+(4.015), (I.01)+(4.016),(I.01)+(4.017), (I.01)+(4.018), (I.01)+(4.019), (I.01)+(4.020),(I.01)+(4.021), (I.01)+(4.022), (I.01)+(4.023), (I.01)+(4.024),(I.01)+(4.025), (I.01)+(5.001), (I.01)+(5.002), (I.01)+(5.003),(I.01)+(5.004), (I.01)+(5.005), (I.01)+(5.006), (I.01)+(5.007),(I.01)+(5.008), (I.01)+(5.009), (I.01)+(5.010), (I.01)+(5.011),(I.01)+(5.012), (I.01)+(5.013), (I.01)+(5.014), (I.01)+(5.015),(I.01)+(5.016), (I.01)+(5.017), (I.01)+(5.018), (I.01)+(5.019),(I.01)+(5.020), (I.01)+(5.021), (I.01)+(5.022), (I.01)+(5.023),(I.01)+(6.001), (I.01)+(6.002), (I.01)+(6.003), (I.01)+(6.004),(I.01)+(7.001), (I.01)+(7.002), (I.01)+(7.003), (I.01)+(7.004),(I.01)+(7.005), (I.01)+(7.006), (I.01)+(8.001), (I.01)+(9.001),(I.01)+(9.002), (I.01)+(9.003), (I.01)+(9.004), (I.01)+(9.005),(I.01)+(9.006), (I.01)+(9.007), (I.01)+(9.008), (I.01)+(9.009),(I.01)+(10.001), (I.01)+(10.002), (I.01)+(10.003), (I.01)+(11.001),(I.01)+(11.002), (I.01)+(12.001), (I.01)+(12.002), (I.01)+(12.003),(I.01)+(12.004), (I.01)+(13.001), (I.01)+(13.002), (I.01)+(13.003),(I.01)+(13.004), (I.01)+(13.005), (I.01)+(13.006), (I.01)+(14.001),(I.01)+(14.002), (I.01)+(15.001), (I.01)+(15.002), (I.01)+(15.003),(I.01)+(15.004), (I.01)+(15.005), (I.01)+(15.006), (I.01)+(15.007),(I.01)+(15.008), (I.01)+(15.009), (I.01)+(15.010), (I.01)+(15.011),(I.01)+(15.012), (I.01)+(15.013), (I.01)+(15.014), (I.01)+(15.015),(I.01)+(15.016), (I.01)+(15.017), (I.01)+(15.018), (I.01)+(15.019),(I.01)+(15.020), (I.01)+(15.021), (I.01)+(15.022), (I.01)+(15.023),(I.01)+(15.024), (I.01)+(15.025), (I.01)+(15.026), (I.01)+(15.027),(I.01)+(15.028), (I.01)+(15.029), (I.01)+(15.030), (I.01)+(15.031),(I.01)+(15.032), (I.01)+(15.033), (I.01)+(15.034), (I.01)+(15.035),(I.01)+(15.036), (I.01)+(15.037), (I.01)+(15.038), (I.01)+(15.039),(I.01)+(15.040), (I.01)+(15.041), (I.01)+(15.042), (I.01)+(15.043),(I.01)+(15.044), (I.01)+(15.045), (I.01)+(15.046), (I.01)+(15.047),(I.01)+(15.048), (I.01)+(15.049), (I.01)+(15.050), (I.01)+(15.051),(I.01)+(15.052), (I.01)+(15.053), (I.01)+(15.054), (I.01)+(15.055),(I.01)+(15.056), (I.01)+(15.057), (I.01)+(15.058), (I.01)+(15.059),(I.01)+(15.060), (I.01)+(15.061), (I.01)+(15.062). (I.01)+(15.063).(I.01)+(15.064). (I.01)+(15.065), (I.01)+15.066), (I.01)+(15.067),(I.01)+(15.068), (I.01)+(15.069), (I.01)+(15.070), (I.01)+(15.071),(I.01)+(15.072), (I.01)+(15.073), (I.01)+(15.074), (I.01)+(15.075),(I.01)+(15.076), (I.01), (I.01)+(15.077), (I.01)+(15.078),(I.01)+(15.079), (I.01)+(15.080), (I.01)+(15.081), (I.01)+(15.082),(I.01)+(15.083), (I.01)+(15.084), (I.01)+(15.085), (I.01)+(15.086),(I.01)+(15.087), (I.01)+(15.088), (I.01)+(15.089), (I.01)+(15.090),(I.01)+(15.091), (I.01)+(15.092), (I.01)+(15.093), (I.01)+(15.094),(I.01)+(15.095), (I.01)+(15.096), (I.01)+(15.097), (I.01)+(15.098),(I.01)+(15.099), (I.01)+(15.100), (I.01)+(15.101), (I.01)+(15.102),(I.01)+(15.103), (I.01)+(15.104), (I.01)+(15.105), (I.01)+(15.106),(I.01)+(15.107), (I.01)+(15.108), (I.01)+(15.109), (I.01)+(15.110),(I.01)+(15.111), (I.01)+(15.112).

In these combinations, the first component is a compound of formula (I)as defined in table I.1 (e.g. I.01) and the second component is afungicide chosen in groups 1 to 15 as defined herein. For instance, thecombination (I.01)+(I.001) corresponds to a combination comprisingcompound I.01 in Table I.1 and cyproconazole (I.001).

In some other embodiments, the compound combinations correspond to theabove described combinations wherein compound (I.01) is replaced withany one of the compounds recited in Table I.1.

The compounds of formula (I), and the fungicide selected from groups (1)to (15), can be present in a weight ratio ranging from 100:1 to 1:100(compound of formula (I):fungicide selected from the groups (1) to(15)), or ranging from 50:1 to 1:50, or ranging from 20:1 to 1:20.Further examples of weight ratio ranges include 95:1 to 1:95, 90:1 to1:90, 85:1 to 1:85, 80:1 to 1:80, 75:1 to 1:75, 70:1 to 1:70, 65:1 to1:65, 60:1 to 1:60, 55:1 to 1:55, 45:1 to 1:45, 40:1 to 1:40, 35:1 to1:35, 30:1 to 1:30, 25:1 to 1:25, 15:1 to 1:15, 10:1 to 1:10, 5:1 to1:5, 4:1 to 1:4, 3:1 to 1:3, 2:1 to 1:2.

A further fungicide chosen in groups 1 to 15 as defined herein may beadded to the compound combinations.

The compound(s) and the composition of the invention may also becombined with one or more biological control agents.

Examples of biological control agents which may be combined with thecompound(s) and the composition of the invention are:

(A) Antibacterial agents selected from the group of:

(A1) bacteria, such as (A1.1) Bacillus subtilis, in particular strainQST713/AQ713 (available as SERENADE OPTI or SERENADE ASO from BayerCropScience LP, US, having NRRL Accession No. B21661 and described inU.S. Pat. No. 6,060,051); (A1.2) Bacillus amyloliquefaciens, inparticular strain D747 (available as Double Nickel™ from Certis, US,having accession number FERM BP-8234 and disclosed in U.S. Pat. No.7,094,592); (A1.3) Bacillus pumilus, in particular strain BU F-33(having NRRL Accession No. 50185); (A1.4) Bacillus subtilis var.amyloliquefaciens strain FZB24 (available as Taegro® from Novozymes,US); (A1.5) a Paenibacillus sp. strain having Accession No. NRRL B-50972or Accession No. NRRL B-67129 and described in International PatentPublication No. WO 2016/154297; and(A2) fungi, such as (A2.1) Aureobasidium pullulans, in particularblastospores of strain DSM14940;(A2.2) Aureobasidium pullulans blastospores of strain DSM 14941; (A2.3)Aureobasidium pullulans, in particular mixtures of blastospores ofstrains DSM14940 and DSM14941;(B) Fungicides selected from the group of:(B1) bacteria, for example (B1.1) Bacillus subtilis, in particularstrain QST713/AQ713 (available as SERENADE OPTI or SERENADE ASO fromBayer CropScience LP, US, having NRRL Accession No. B21661 and describedin U.S. Pat. No. 6,060,051); (B1.2) Bacillus pumilus, in particularstrain QST2808 (available as SONATA® from Bayer CropScience LP, US,having Accession No. NRRL B-30087 and described in U.S. Pat. No.6,245,551); (B1.3) Bacillus pumilus, in particular strain GB34(available as Yield Shield® from Bayer AG, DE); (B1.4) Bacillus pumilus,in particular strain BU F-33 (having NRRL Accession No. 50185); (B1.5)Bacillus amyloliquefaciens, in particular strain D747 (available asDouble Nickel™ from Certis, US, having accession number FERM BP-8234 anddisclosed in U.S. Pat. No. 7,094,592); (B1.6) Bacillus subtilis Y1336(available as BIOBAC® WP from Bion-Tech, Taiwan, registered as abiological fungicide in Taiwan under Registration Nos. 4764, 5454, 5096and 5277); (B1.7) Bacillus amyloliquefaciens strain MBI 600 (availableas SUBTILEX from BASF SE); (B1.8) Bacillus subtilis strain GB03(available as Kodiak® from Bayer AG, DE); (B1.9) Bacillus subtilis var.amyloliquefaciens strain FZB24 (available from Novozymes BiologicalsInc., Salem, Va. or Syngenta Crop Protection, LLC, Greensboro, N.C. asthe fungicide TAEGRO® or TAEGRO® ECO (EPA Registration No. 70127-5);(B1.10) Bacillus mycoides, isolate J (available as BmJ TGAI or WG fromCertis USA); (B1.11) Bacillus licheniformis, in particular strain SB3086(available as EcoGuard™ Biofungicide and Green Releaf from Novozymes);(B1.12) a Paenibacillus sp. strain having Accession No. NRRL B-50972 orAccession No. NRRL B-67129 and described in International PatentPublication No. WO 2016/154297.

In some embodiments, the biological control agent is a Bacillus subtilisor Bacillus amyloliquefaciens strain that produces a fengycin orplipastatin-type compound, an iturin-type compound, and/or asurfactin-type compound. For background, see the following reviewarticle: Ongena, M., et al., “Bacillus Lipopeptides: Versatile Weaponsfor Plant Disease Biocontrol,” Trends in Microbiology, Vol 16, No. 3,March 2008, pp. 115-125. Bacillus strains capable of producinglipopeptides include Bacillus subtilis QST713 (available as SERENADEOPTI or SERENADE ASO from Bayer CropScience LP, US, having NRRLAccession No. B21661 and described in U.S. Pat. No. 6,060,051), Bacillusamyloliquefaciens strain D747 (available as Double Nickel™ from Certis,US, having accession number FERM BP-8234 and disclosed in U.S. Pat. No.7,094,592); Bacillus subtilis MBI600 (available as SUBTILEX® from BeckerUnderwood, US EPA Reg. No. 71840-8); Bacillus subtilis Y1336 (availableas BIOBAC® WP from Bion-Tech, Taiwan, registered as a biologicalfungicide in Taiwan under Registration Nos. 4764, 5454, 5096 and 5277);Bacillus amyloliquefaciens, in particular strain FZB42 (available asRFIIZOVITAL® from ABiTEP, DE); and Bacillus subtilis var.amyloliquefaciens FZB24 (available from Novozymes Biologicals Inc.,Salem, Va. or Syngenta Crop Protection, LLC, Greensboro, N.C. as thefungicide TAEGRO® or TAEGRO® ECO (EPA Registration No. 70127-5); and

(B2) fungi, for example: (B2.1) Coniothyrium minitans, in particularstrain CON/M/91-8 (Accession No. DSM-9660; e.g. Contans® from Bayer);(B2.2) Metschnikowia fructicola, in particular strain NRRL Y-30752 (e.g.Shemer®); (B2.3) Microsphaeropsis ochracea (e.g. Microx® from Prophyta);(B2.5) Trichoderma spp., including Trichoderma atroviride, strain SC1described in International Application No. PCT/IT2008/000196); (B2.6)Trichoderma harzianum rifaistrain KRL-AG2 (also known as strain T-22,/ATCC 208479, e.g. PLANTSHIELD T-22G, Rootshield®, and TurfShield fromBioWorks, US); (B2.14) Gliocladium roseum, strain 321U from W. F.Stoneman Company LLC; (B2.35) Talaromyces flavus, strain V117b; (B2.36)Trichoderma asperellum, strain ICC 012 from Isagro; (B2.37) Trichodermaasperellum, strain SKT-1 (e.g. ECO-HOPE® from Kumiai Chemical Industry);(B2.38) Trichoderma atroviride, strain CNCM 1-1237 (e.g. Esquive® WPfrom Agrauxine, FR); (B2.39) Trichoderma atroviride, strain no.V08/002387; (B2.40) Trichoderma atroviride, strain NMI no. V08/002388;(B2.41) Trichoderma atroviride, strain NMI no. V08/002389; (B2.42)Trichoderma atroviride, strain NMI no. V08/002390; (B2.43) Trichodermaatroviride, strain LC52 (e.g. Tenet by Agrimm Technologies Limited);(B2.44) Trichoderma atroviride, strain ATCC 20476 (IMI 206040); (B2.45)Trichoderma atroviride, strain T11 (IMI352941/CECT20498); (B2.46)Trichoderma harmatum, (B2.47) Trichoderma harzianum, (B2.48) Trichodermaharzianum rifai T39 (e.g. Trichodex® from Makhteshim, US); (B2.49)Trichoderma harzianum, in particular, strain KD (e.g. Trichoplus fromBiological Control Products, SA (acquired by Becker Underwood)); (B2.50)Trichoderma harzianum, strain ITEM 908 (e.g. Trianum-P from Koppert);(B2.51) Trichoderma harzianum, strain TH35 (e.g. Root-Pro by Mycontrol);(B2.52) Trichoderma virens (also known as Gliocladium virens), inparticular strain GL-21 (e.g. SoilGard 12G by Certis, US); (B2.53)Trichoderma viride, strain TV1 (e.g. Trianum-P by Koppert); (B2.54)Ampelomyces quisqualis, in particular strain AQ 10 (e.g. AQ 10® byIntrachemBio Italia); (B2.56) Aureobasidium pullulans, in particularblastospores of strain DSM14940; (B2.57) Aureobasidium pullulans, inparticular blastospores of strain DSM 14941; (B2.58) Aureobasidiumpullulans, in particular mixtures of blastospores of strains DSM14940and DSM 14941 (e.g. Botector® by bio-ferm, CH); (B2.64) Cladosporiumcladosporioides, strain H39 (by Stichting Dienst LandbouwkundigOnderzoek); (B2.69) Gliocladium catenulatum (Synonym: Clonostachys roseaf. catenulate) strain J1446 (e.g. Prestop® by AgBio Inc. and also e.g.Primastop® by Kemira Agro Oy); (B2.70) Lecanicillium lecanii (formerlyknown as Verticillium lecanii) conidia of strain KV01 (e.g. Vertalec® byKoppert/Arysta); (B2.71) Penicillium vermiculatum; (B2.72) Pichiaanomala, strain WRL-076 (NRRL Y-30842); (B2.75) Trichoderma atroviride,strain SKT-1 (FERM P-16510); (B2.76) Trichoderma atroviride, strainSKT-2 (FERM P-16511); (B2.77) Trichoderma atroviride, strain SKT-3 (FERMP-17021); (B2.78) Trichoderma gamsii (formerly T. viride), strain ICC080(IMI CC 392151 CABI, e.g. BioDerma by AGROBIOSOL DE MEXICO, S.A. DEC.V.); (B2.79) Trichoderma harzianum, strain DB 103 (e.g., T-Gro 7456 byDagutat Biolab); (B2.80) Trichoderma polysporum, strain IMI 206039 (e.g.Binab TF WP by BINAB Bio-Innovation AB, Sweden); (B2.81) Trichodermastromaticum (e.g. Tricovab by Ceplac, Brazil); (B2.83) Ulocladiumoudemansii, in particular strain HRU3 (e.g. Botry-Zen® by Botry-Zen Ltd,NZ); (B2.84) Verticillium albo-atrum (formerly V. dahliae), strainWCS850 (CBS 276.92; e.g. Dutch Trig by Tree Care Innovations); (B2.86)Verticillium chlamydosporium, (B2.87) mixtures of Trichoderma asperellumstrain ICC 012 and Trichoderma gamsii strain ICC 080 (product known ase.g. BIO-TAM™ from Bayer CropScience LP, US).

Further examples of biological control agents which may be combined withthe compound(s) and the composition of the invention are:

bacteria selected from the group consisting of Bacillus cereus, inparticular B. cereus strain CNCM I-1562 and Bacillus firmus, strain1-1582 (Accession number CNCM 1-1582), Bacillus subtilis strain OST30002 (Accession No. NRRL B-50421), Bacillus thuringiensis, inparticular B. thuringiensis subspecies israelensis (serotype H-14),strain AM65-52 (Accession No. ATCC 1276), B. thuringiensis subsp.aizawai, in particular strain ABTS-1857 (SD-1372), B. thuringiensissubsp. kurstaki strain HD-1, B. thuringiensis subsp. tenebrionis strainNB 176 (SD-5428), Pasteuria penetrans, Pasteuria spp. (Rotylenchulusreniformis nematode)-PR3 (Accession Number ATCC SD-5834), Streptomycesmicroflavus strain AQ6121 (=QRD 31.013, NRRL B-50550), and Streptomycesgalbus strain AQ 6047 (Accession Number NRRL 30232);fungi and yeasts selected from the group consisting of Beauveriabassiana, in particular strain ATCC 74040, Lecanicillium spp., inparticular strain HRO LEC 12, Metarhizium anisopliae, in particularstrain F52 (DSM3884 or ATCC 90448), Paecilomyces fumosoroseus (now:Isaria fumosorosea), in particular strain IFPC 200613, or strain Apopka97 (Accession No. ATCC 20874), and Paecilomyces lilacinus, in particularP. lilacinus strain 251 (AGAL 89/030550);viruses selected from the group consisting of Adoxophyes orana (summerfruit tortrix) granulosis virus (GV), Cydia pomonella (codling moth)granulosis virus (GV), Helicoverpa armigera (cotton bollworm) nuclearpolyhedrosis virus (NPV), Spodoptera exigua (beet armyworm) mNPV,Spodoptera frugiperda (fall armyworm) mNPV, and Spodoptera littoralis(African cotton leafworm) NPV.bacteria and fungi which can be added as ‘inoculant’ to plants or plantparts or plant organs and which, by virtue of their particularproperties, promote plant growth and plant health. Examples are:Agrobacterium spp., Azorhizobium caulinodans. Azospirillum spp.,Azotobacter spp., Bradyrhizobium spp., Burkholderia spp., in particularBurkholderia cepacia (formerly known as Pseudomonas cepacia), Gigasporaspp., or Gigaspora monosporum. Glomus spp., Laccaria spp., Lactobacillusbuchneri, Paraglomus spp., Pisolithus tinctorus, Pseudomonas spp.,Rhizobium spp., in particular Rhizobium trifolii, Rhizopogon spp.,Scleroderma spp., Suillus spp., and Streptomyces spp.plant extracts and products formed by microorganisms including proteinsand secondary metabolites which can be used as biological controlagents, such as Allium sativum, Artemisia absinthium, azadirachtin,Biokeeper WP, Cassia nigricans, Celastrus angulatus, Chenopodiumanthelminticum, chitin, Armour-Zen, Dryopteris filix-mas, Equisetumarvense, Fortune Aza, Fungastop, Pleads Up (Chenopodium quinoa saponinextract), Pyrethrum/Pyrethrins, Quassia amara, Quercus, Quillaja,Regalia, “Requiem™ Insecticide”, rotenone, ryania/ryanoide, Symphytumofficinale, Tanacetum vulgare, thymol, Triad 70, TriCon, Tropaeulummajus, Urtica dioica, Veratrin, Viscum album, Brassicaceae extract, inparticular oilseed rape powder or mustard powder.

Examples of insecticides, acaricides and nematicides, respectively,which could be mixed with the compound(s) and the composition of theinvention are:

(1) Acetylcholinesterase (AChE) inhibitors, such as, for example,carbamates, for example alanycarb, aldicarb, bendiocarb, benfuracarb,butocarboxim, butoxycarboxim, carbaryl, carbofuran, carbosulfan,ethiofencarb, fenobucarb, formetanate, furathiocarb, isoprocarb,methiocarb, methomyl, metolcarb, oxamyl, pirimicarb, propoxur,thiodicarb, thiofanox, triazamate, trimethacarb, XMC and xylylcarb; ororganophosphates, for example acephate, azamethiphos, azinphos-ethyl,azinphos-methyl, cadusafos, chlorethoxyfos, chlorfenvinphos,chlormephos, chlorpyrifos-methyl, coumaphos, cyanophos,demeton-S-methyl, diazinon, dichlorvos/DDVP, dicrotophos, dimethoate,dimethylvinphos, disulfoton, EPN, ethion, ethoprophos, famphur,fenamiphos, fenitrothion, fenthion, fosthiazate, heptenophos, imicyafos,isofenphos, isopropyl O-(methoxyaminothiophosphoryl) salicylate,isoxathion, malathion, mecarbam, methamidophos, methidathion, mevinphos,monocrotophos, naled, omethoate, oxydemeton-methyl, parathion-methyl,phenthoate, phorate, phosalone, phosmet, phosphamidon, phoxim,pirimiphos-methyl, profenofos, propetamphos, prothiofos, pyraclofos,pyridaphenthion, quinalphos, sulfotep, tebupirimfos, temephos, terbufos,tetrachlorvinphos, thiometon, triazophos, triclorfon and vamidothion.(2) GABA-gated chloride channel blockers, such as, for example,cyclodiene-organochlorines, for example chlordane and endosulfan orphenylpyrazoles (fiproles), for example ethiprole and fipronil.(3) Sodium channel modulators, such as, for example, pyrethroids, e.g.acrinathrin, allethrin, d-cis-trans allethrin, d-trans allethrin,bifenthrin, bioallethrin, bioallethrin s-cyclopentenyl isomer,bioresmethrin, cycloprothrin, cyfluthrin, beta-cyfluthrin, cyhalothrin,lambda-cyhalothrin, gamma-cyhalothrin, cypermethrin, alpha-cypermethrin,beta-cypermethrin, theta-cypermethrin, zeta-cypermethrin, cyphenothrin[(1R)-trans-isomer], deltamethrin, empenthrin [(EZ)-(1R)-isomer],esfenvalerate, etofenprox, fenpropathrin, fenvalerate, flucythrinate,flumethrin, tau-fluvalinate, halfenprox, imiprothrin, kadethrin,momfluorothrin, permethrin, phenothrin [(1R)-trans-isomer], prallethrin,pyrethrins (pyrethrum), resmethrin, silafluofen, tefluthrin,tetramethrin, tetramethrin [(1R)-isomer)], tralomethrin andtransfluthrin or DDT or methoxychlor.(4) Nicotinic acetylcholine receptor (nAChR) competitive modulators,such as, for example, neonicotinoids, e.g. acetamiprid, clothianidin,dinotefuran, imidacloprid, nitenpyram, thiacloprid and thiamethoxam ornicotine or sulfoxaflor or flupyradifurone.(5) Nicotinic acetylcholine receptor (nAChR) allosteric modulators, suchas, for example, spinosyns, e.g. spinetoram and spinosad.(6) Glutamate-gated chloride channel (GluCl) allosteric modulators, suchas, for example, avermectins/milbemycins, for example abamectin,emamectin benzoate, lepimectin and milbemectin.(7) Juvenile hormone mimics, such as, for example, juvenile hormoneanalogues, e.g. hydroprene, kinoprene and methoprene or fenoxycarb orpyriproxyfen.(8) Miscellaneous non-specific (multi-site) inhibitors, such as, forexample, alkyl halides, e.g. methyl bromide and other alkyl halides; orchloropicrine or sulphuryl fluoride or borax or tartar emetic or methylisocyanate generators, e.g. diazomet and metam.(9) Modulators of Chordotonal Organs, such as, for example pymetrozineor flonicamid.(10) Mite growth inhibitors, such as, for example clofentezine,hexythiazox and diflovidazin or etoxazole.(11) Microbial disruptors of the insect gut membrane, such as, forexample Bacillus thuringiensis subspecies israelensis, Bacillussphaericus, Bacillus thuringiensis subspecies aizawai, Bacillusthuringiensis subspecies kurstaki, Bacillus thuringiensis subspeciestenebrionis, and B.t. plant proteins: Cry1Ab, Cry1Ac, Cry1 Fa,Cry1A.105, Cry2Ab, Vip3A, mCry3A, Cry3Ab, Cry3Bb, Cry34Ab1/35Ab1.(12) Inhibitors of mitochondrial ATP synthase, such as, ATP disruptorssuch as, for example, diafenthiuron or organotin compounds, for exampleazocyclotin, cyhexatin and fenbutatin oxide or propargite or tetradifon.(13) Uncouplers of oxidative phosphorylation via disruption of theproton gradient, such as, for example, chlorfenapyr, DNOC andsulfluramid.(14) Nicotinic acetylcholine receptor channel blockers, such as, forexample, bensultap, cartap hydrochloride, thiocylam, andthiosultap-sodium.(15) Inhibitors of chitin biosynthesis, type 0, such as, for example,bistrifluron, chlorfluazuron, diflubenzuron, flucycloxuron,flufenoxuron, hexaflumuron, lufenuron, novaluron, noviflumuron,teflubenzuron and triflumuron.(16) Inhibitors of chitin biosynthesis, type 1, for example buprofezin.(17) Moulting disruptor (in particular for Diptera, i.e. dipterans),such as, for example, cyromazine.(18) Ecdysone receptor agonists, such as, for example, chromafenozide,halofenozide, methoxyfenozide and tebufenozide.(19) Octopamine receptor agonists, such as, for example, amitraz.(20) Mitochondrial complex III electron transport inhibitors, such as,for example, hydramethylnone or acequinocyl or fluacrypyrim.(21) Mitochondrial complex I electron transport inhibitors, such as, forexample from the group of the METI acaricides, e.g. fenazaquin,fenpyroximate, pyrimidifen, pyridaben, tebufenpyrad and tolfenpyrad orrotenone (Derris).(22) Voltage-dependent sodium channel blockers, such as, for exampleindoxacarb or metaflumizone.(23) Inhibitors of acetyl CoA carboxylase, such as, for example,tetronic and tetramic acid derivatives, e.g. spirodiclofen, spiromesifenand spirotetramat.(24) Mitochondrial complex IV electron transport inhibitors, such as,for example, phosphines, e.g. aluminium phosphide, calcium phosphide,phosphine and zinc phosphide or cyanides, e.g. calcium cyanide,potassium cyanide and sodium cyanide.(25) Mitochondrial complex II electron transport inhibitors, such as,for example, befa-ketonitrile derivatives, e.g. cyenopyrafen andcyflumetofen and carboxanilides, such as, for example, pyflubumide.(28) Ryanodine receptor modulators, such as, for example, diamides, e.g.chlorantraniliprole, cyantraniliprole and flubendiamide,further active compounds such as, for example, Afidopyropen, Afoxolaner,Azadirachtin, Benclothiaz, Benzoximate, Bifenazate, Broflanilide,Bromopropylate, Chinomethionat, Chloroprallethrin, Cryolite,Cyclaniliprole, Cycloxaprid, Cyhalodiamide, Dicloromezotiaz, Dicofol,epsilon-Metofluthrin, epsilon-Momfluthrin, Flometoquin,Fluazaindolizine, Fluensulfone, Flufenerim, Flufenoxystrobin,Flufiprole, Fluhexafon, Fluopyram, Fluralaner, Fluxametamide,Fufenozide, Guadipyr, Heptafluthrin, Imidaclothiz, Iprodione,kappa-Bifenthrin, kappa-Tefluthrin, Lotilaner, Meperfluthrin,Paichongding, Pyridalyl, Pyrifluquinazon, Pyriminostrobin,Spirobudiclofen, Tetramethylfluthrin, Tetraniliprole,Tetrachlorantraniliprole, Tigolaner, Tioxazafen, Thiofluoximate,Triflumezopyrim and iodomethane; furthermore preparations based onBacillus firmus (1-1582, BioNeem, Votivo), and also the followingcompounds:1-{2-fluoro-4-methyl-5-[(2,2,2-trifluoroethyl)sulphinyl]phenyl}-3-(trifluoromethyl)-1H-1,2,4-triazole-5-amine(known from WO2006/043635) (CAS 885026-50-6),{1′-[(2E)-3-(4-chlorophenyl)prop-2-en-1-yl]-5-fluorospiro[indol-3,4′-piperidin]-1(2H)-yl}(2-chloropyridin-4-yl)methanone (known from WO2003/106457) (CAS637360-23-7),2-chloro-N-[2-{1-[(2E)-3-(4-chlorophenyl)prop-2-en-1-yl]piperidin-4-yl}-4-(trifluoromethyl)phenyl]isonicotinamide(known from WO2006/003494) (CAS 872999-66-1),3-(4-chloro-2,6-dimethylphenyl)-4-hydroxy-8-methoxy-1,8-diazaspiro[4.5]dec-3-en-2-one(known from WO 2010052161) (CAS 1225292-17-0),3-(4-chloro-2,6-dimethylphenyl)-8-methoxy-2-oxo-1,8-diazaspiro[4.5]dec-3-en-4-ylethyl carbonate (known from EP2647626) (CAS 1440516-42-6),4-(but-2-yn-1-yloxy)-6-(3,5-dimethylpiperidin-1-yl)-5-fluoropyrimidine(known from WO2004/099160) (CAS 792914-58-0), PF1364 (known fromJP2010/018586) (CAS 1204776-60-2),N-[(2E)-1-[(6-chloropyridin-3-yl)methyl]pyridin-2(1H)-ylidene]-2,2,2-trifluoroacetamide(known from WO2012/029672) (CAS 1363400-41-2),(3E)-3-[1-[(6-chloro-3-pyridyl)methyl]-2-pyridylidene]-1,1,1-trifluoro-propan-2-one(known from WO2013/144213) (CAS 1461743-15-6),N-[3-(benzylcarbamoyl)-4-chlorophenyl]-1-methyl-3-(pentafluoroethyl)-4-(trifluoromethyl)-1H-pyrazole-5-carboxamide(known from WO2010/051926) (CAS 1226889-14-0),5-bromo-4-chloro-N-[4-chloro-2-methyl-6-(methylcarbamoyl)phenyl]-2-(3-chloro-2-pyridyl)pyrazole-3-carboxamide(known from CN103232431) (CAS 1449220-44-3),4-[5-(3,5-dichlorophenyl)-4,5-dihydro-5-(trifluoromethyl)-3-isoxazolyl]-2-methyl-N-(cis-1-oxido-3-thietanyl)-benzamide,4-[5-(3,5-dichlorophenyl)-4,5-dihydro-5-(trifluoromethyl)-3-isoxazolyl]-2-methyl-N-(trans-1-oxido-3-thietanyl)-benzamideand4-[(5S)-5-(3,5-dichlorophenyl)-4,5-dihydro-5-(trifluoromethyl)-3-isoxazolyl]-2-methyl-N-(cis-1-oxido-3-thietanyl)benzamide(known from WO 2013/050317 A1) (CAS 1332628-83-7),N-[3-chloro-1-(3-pyridinyl)-1H-pyrazol-4-yl]-N-ethyl-3-[(3,3,3-trifluoropropyl)sulfinyl]-propanamide,(+)-N-[3-chloro-1-(3-pyridinyl)-1H-pyrazol-4-yl]-N-ethyl-3-[(3,3,3-trifluoropropyl)sulfinyl]-propanamide and(−)-N-[3-chloro-1-(3-pyridinyl)-1H-pyrazol-4-yl]-N-ethyl-3-[(3,3,3-trifluoropropyl)sulfinyl]-propanamide(known from WO 2013/162715 A2, WO 2013/162716 A2, US 2014/0213448 A1)(CAS 1477923-37-7),5-[[(2E)-3-chloro-2-propen-1-yl]amino]-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-4-[(trifluoromethyl)sulfinyl]-1H-pyrazole-3-carbonitrile(known from CN 101337937 A) (CAS 1105672-77-2),3-bromo-N-[4-chloro-2-methyl-6-[(methylamino)thioxomethyl]phenyl]-1-(3-chloro-2-pyridinyl)-1H-pyrazole-5-carboxamide,(Liudaibenjiaxuanan, known from CN 103109816 A) (CAS 1232543-85-9);N-[4-chloro-2-[[(1,1-dimethylethyl)amino]carbonyl]-6-methylphenyl]-1-(3-chloro-2-pyridinyl)-3-(fluoromethoxy)-1H-Pyrazole-5-carboxamide(known from WO 2012/034403 A1) (CAS 1268277-22-0),N-[2-(5-amino-1,3,4-thiadiazol-2-yl)-4-chloro-6-methylphenyl]-3-bromo-1-(3-chloro-2-pyridinyl)-1H-pyrazole-5-carboxamide(known from WO 2011/085575 A1) (CAS 1233882-22-8),4-[3-[2,6-dichloro-4-[(3,3-dichloro-2-propen-1-yl)oxy]phenoxy]propoxy]-2-methoxy-6-(trifluoromethyl)-pyrimidine(known from CN 101337940 A) (CAS 1108184-52-6); (2E)- and2(Z)-2-[2-(4-cyanophenyl)-1-[3-(trifluoromethyl)phenyl]ethylidene]-N-[4-(difluoromethoxy)phenyl]-hydrazinecarboxamide(known from CN 101715774 A) (CAS 1232543-85-9);3-(2,2-dichloroethenyl)-2,2-dimethyl-4-(1H-benzimidazol-2-yl)phenyl-cyclopropanecarboxylicacid ester (known from CN 103524422 A) (CAS 1542271-46-4);(4aS)-7-chloro-2,5-dihydro-2-[[(methoxycarbonyl)[4-[(trifluoromethyl)thio]phenyl]amino]carbonyl]-indeno[1,2-e][1,3,4]oxadiazine-4a(3AV)-carboxylicacid methyl ester (known from CN 102391261 A) (CAS 1370358-69-2);6-deoxy-3-O-ethyl-2,4-di-O-methyl-,1-[N-[4-[1-[4-(1,1,2,2,2-pentafluoroethoxy)phenyl]-1H-1,2,4-triazol-3-yl]phenyl]carbamate]-α-L-mannopyranose(known from US 2014/0275503 A1) (CAS 1181213-14-8);8-(2-cyclopropylmethoxy-4-trifluoromethyl-phenoxy)-3-(6-trifluoromethyl-pyridazin-3-yl)-3-aza-bicyclo[3.2.1]octane(CAS 1253850-56-4),(8-anti)-8-(2-cyclopropylmethoxy-4-trifluoromethyl-phenoxy)-3-(6-trifluoromethyl-pyridazin-3-yl)-3-aza-bicyclo[3.2.1]octane(CAS 933798-27-7),(8-syn)-8-(2-cyclopropylmethoxy-4-trifluoromethyl-phenoxy)-3-(6-trifluoromethyl-pyridazin-3-yl)-3-aza-bicyclo[3.2.1]octane(known from WO 2007040280 A1, WO 2007040282 A1) (CAS 934001-66-8),N-[3-chloro-1-(3-pyridinyl)-1H-pyrazol-4-yl]-N-ethyl-3-[(3,3,3-trifluoropropyl)thio]-propanamide(known from WO 2015/058021 A1, WO 2015/058028 A1) (CAS 1477919-27-9) andN-[4-(aminothioxomethyl)-2-methyl-6-[(methylamino)carbonyl]phenyl]-3-bromo-1-(3-chloro-2-pyridinyl)-1H-pyrazole-5-carboxamide(known from CN 103265527 A) (CAS 1452877-50-7),5-(1,3-dioxan-2-yl)-4-[[4-(trifluoromethyl)phenyl]methoxy]-pyrimidine(known from WO 2013/115391 A1) (CAS 1449021-97-9),3-(4-chloro-2,6-dimethylphenyl)-4-hydroxy-8-methoxy-1-methyl-1,8-diazaspiro[4.5]dec-3-en-2-one(known from WO 2010/066780 A1, WO 2011/151146 A1) (CAS 1229023-34-0),3-(4-chloro-2,6-dimethylphenyl)-8-methoxy-1-methyl-1,8-diazaspiro[4.5]decane-2,4-dione(known from WO 2014/187846 A1) (CAS 1638765-58-8),3-(4-chloro-2,6-dimethylphenyl)-8-methoxy-1-methyl-2-oxo-1,8-diazaspiro[4.5]dec-3-en-4-yl-carbonic acid ethyl ester (known from WO2010/066780 A1, WO 2011151146 A1) (CAS 1229023-00-0),N-[1-[(6-chloro-3-pyridinyl)methyl]-2(1H)-pyridinylidene]-2,2,2-trifluoro-acetamide(known from DE 3639877 A1, WO 2012029672 A1) (CAS 1363400-41-2),[N(E)]-N-[1-[(6-chloro-3-pyridinyl)methyl]-2(1H)-pyridinylidene]-2,2,2-trifluoro-acetamide,(known from WO 2016005276 A1) (CAS 1689566-03-7),[N(Z)]—N-[1-[(6-chloro-3-pyridinyl)methyl]-2(1H)-pyridinylidene]-2,2,2-trifluoro-acetamide,(CAS 1702305-40-5),3-endo-3-[2-propoxy-4-(trifluoromethyl)phenoxy]-9-[[5-(trifluoromethyl)-2-pyridinyl]oxy]-9-azabicyclo[3.3.1]nonane(known from WO 2011/105506 A1, WO 2016/133011 A1) (CAS 1332838-17-1).

Examples of safeners which could be mixed with the compound(s) and thecomposition of the invention are, for example, benoxacor, cloquintocet(-mexyl), cyometrinil, cyprosulfamide, dichlormid, fenchlorazole(-ethyl), fenclorim, flurazole, fluxofenim, furilazole, isoxadifen(-ethyl), mefenpyr (-diethyl), naphthalic anhydride, oxabetrinil,2-methoxy-N-({4-[(methylcarbamoyl)amino]phenyl}-sulphonyl)benzamide (CAS129531-12-0), 4-(dichloroacetyl)-1-oxa-4-azaspiro[4.5]decane (CAS71526-07-3), 2,2,5-trimethyl-3-(dichloroacetyl)-1,3-oxazolidine (CAS52836-31-4).

Examples of herbicides which could be mixed with the compound(s) and thecomposition of the invention are:

Acetochlor, acifluorfen, acifluorfen-sodium, aclonifen, alachlor,allidochlor, alloxydim, alloxydim-sodium, ametryn, amicarbazone,amidochlor, amidosulfuron,4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methylphenyl)-5-fluoropyridine-2-carboxylicacid, aminocyclopyrachlor, aminocyclopyrachlor-potassium,aminocyclopyrachlor-methyl, aminopyralid, amitrole, ammoniumsulfamate,anilofos, asulam, atrazine, azafenidin, azimsulfuron, beflubutamid,benazolin, benazolin-ethyl, benfluralin, benfuresate, bensulfuron,bensulfuron-methyl, bensulide, bentazone, benzobicyclon, benzofenap,bicyclopyron, bifenox, bilanafos, bilanafos-sodium, bispyribac,bispyribac-sodium, bromacil, bromobutide, bromofenoxim, bromoxynil,bromoxynil-butyrate, -potassium, -heptanoate, and -octanoate,busoxinone, butachlor, butafenacil, butamifos, butenachlor, butralin,butroxydim, butylate, cafenstrole, carbetamide, carfentrazone,carfentrazone-ethyl, chloramben, chlorbromuron, chlorfenac,chlorfenac-sodium, chlorfenprop, chlorflurenol, chlorflurenol-methyl,chloridazon, chlorimuron, chlorimuron-ethyl, chlorophthalim,chlorotoluron, chlorthal-dimethyl, chlorsulfuron, cinidon,cinidon-ethyl, cinmethylin, cinosulfuron, clacyfos, clethodim,clodinafop, clodinafop-propargyl, clomazone, clomeprop, clopyralid,cloransulam, cloransulam-methyl, cumyluron, cyanamide, cyanazine,cycloate, cyclopyrimorate, cyclosulfamuron, cycloxydim, cyhalofop,cyhalofop-butyl, cyprazine, 2,4-D, 2,4-D-butotyl, -butyl,-dimethylammonium, -diolamin, -ethyl, -2-ethylhexyl, -isobutyl,-isooctyl, -isopropyl-ammonium, -potassium, -triisopropanolammonium, and-trolamine, 2,4-DB, 2,4-DB-butyl, -dimethyl-ammonium, -isooctyl,-potassium, and -sodium, daimuron (dymron), dalapon, dazomet, n-decanol,desmedipham, detosyl-pyrazolate (DTP), dicamba, dichlobenil,2-(2,4-dichlorobenzyl)-4,4-dimethyl-1,2-oxazolidin-3-one,2-(2,5-dichlorobenzyl)-4,4-dimethyl-1,2-oxazolidin-3-one, dichlorprop,dichlorprop-P, diclofop, diclofop-methyl, diclofop-P-methyl, diclosulam,difenzoquat, diflufenican, diflufenzopyr, diflufenzopyr-sodium,dimefuron, dimepiperate, dimethachlor, dimethametryn, dimethenamid,dimethenamid-P, dimetrasulfuron, dinitramine, dinoterb, diphenamid,diquat, diquat-dibromid, dithiopyr, diuron, DNOC, endothal, EPTC,esprocarb, ethalfluralin, ethametsulfuron, etha-metsulfuron-methyl,ethiozin, ethofumesate, ethoxyfen, ethoxyfen-ethyl, ethoxysulfuron,etobenzanid, F-9600, F-5231, i.e.N-{2-chloro-4-fluoro-5-[4-(3-fluoropropyl)-5-oxo-4,5-dihydro-1H-tetrazol-1-yl]phenyl}ethanesulfonamide,F-7967, i. e.3-[7-chloro-5-fluoro-2-(trifluoromethyl)-1H-benzimidazol-4-yl]-1-methyl-6-(trifluoromethyl)pyrimidine-2,4(1H,3H)-dione,fenoxaprop, fenoxaprop-P, fenoxaprop-ethyl, fenoxaprop-P-ethyl,fenoxasulfone, fenquinotrione, fentrazamide, flamprop,flamprop-M-isopropyl, flamprop-M-methyl, flazasulfuron, florasulam,fluazifop, fluazifop-P, fluazifop-butyl, fluazifop-P-butyl,flucarbazone, flucarbazone-sodium, flucetosulfuron, fluchloralin,flufenacet, flufenpyr, flufenpyr-ethyl, flumetsulam, flumiclorac,flumiclorac-pentyl, flumioxazin, fluometuron, flurenol, flurenol-butyl,-dimethylammonium and -methyl, fluoroglycofen, fluoroglycofen-ethyl,flupropanate, flupyr-sulfuron, flupyrsulfuron-methyl-sodium, fluridone,flurochloridone, fluroxypyr, fluroxypyr-meptyl, flurtamone, fluthiacet,fluthiacet-methyl, fomesafen, fomesafen-sodium, foramsulfuron, fosamine,glufosinate, glufosinate-ammonium, glufosinate-P-sodium,glufosinate-P-ammonium, glufosinate-P-sodium, glyphosate,glyphosate-ammonium, -isopropylammonium, -diammonium, -dimethylammonium,-potassium, -sodium, and -trimesium, H-9201, i.e.O-(2,4-dimethyl-6-nitrophenyl) O-ethyl isopropylphosphoramidothioate,halauxifen, halauxifen-methyl, halosafen, halosulfuron,halosulfuron-methyl, haloxyfop, haloxyfop-P, haloxyfop-ethoxyethyl,haloxyfop-P-ethoxyethyl, haloxyfop-methyl, haloxyfop-P-methyl,hexazinone, HW-02, i.e. 1-(dimethoxyphosphoryl)ethyl-(2,4-dichlorophenoxy)acetate, imazamethabenz,imazamethabenz-methyl, imazamox, imazamox-ammonium, imazapic,imazapic-ammonium, imazapyr, imazapyr-isopropylammonium, imazaquin,imazaquin-ammonium, imazethapyr, imazethapyr-immonium, imazosulfuron,indanofan, indaziflam, iodosulfuron, iodosulfuron-methyl-sodium,ioxynil, ioxynil-octanoate, -potassium and -sodium, ipfencarbazone,isoproturon, isouron, isoxaben, isoxaflutole, karbutilate, KUH-043, i.e.3-({[5-(difluoromethyl)-1-methyl-3-(trifluoromethyl)-1H-pyrazol-4-yl]methyl}sulfonyl)-5,5-dimethyl-4,5-dihydro-1,2-oxazole,ketospiradox, lactofen, lenacil, linuron, MCPA, MCPA-butotyl,-dimethylammonium, -2-ethylhexyl, -isopropylammonium, -potassium, and-sodium, MCPB, MCPB-methyl, -ethyl, and -sodium, mecoprop,mecoprop-sodium, and -butotyl, mecoprop-P, mecoprop-P-butotyl,-dimethylammonium, -2-ethylhexyl, and -potassium, mefenacet, mefluidide,mesosulfuron, mesosulfuron-methyl, mesotrione, methabenzthiazuron,metam, metamifop, metamitron, metazachlor, metazosulfuron,methabenz-thiazuron, methiopyrsulfuron, methiozolin, methylisothiocyanate, metobromuron, metolachlor, S-metolachlor, metosulam,metoxuron, metribuzin, metsulfuron, metsulfuron-methyl, molinat,mono-linuron, monosulfuron, monosulfuron-ester, MT-5950, i.e.N-(3-chloro-4-isopropylphenyl)-2-methylpentan amide, NGGC-011,napropamide, NC-310, i.e.[5-(benzyloxy)-1-methyl-1H-pyrazol-4-yl](2,4-dichlorophenyl)methanone,neburon, nicosulfuron, nonanoic acid (pelargonic acid), norflurazon,oleic acid (fatty acids), orbencarb, orthosulfamuron, oryzalin,oxadiargyl, oxadiazon, oxasulfuron, oxaziclomefon, oxyfluorfen,paraquat, paraquat dichloride, pebulate, pendimethalin, penoxsulam,pentachlorophenol, pentoxazone, pethoxamid, petroleum oils,phenmedipham, picloram, picolinafen, pinoxaden, piperophos,pretilachlor, primisulfuron, primisulfuron-methyl, prodiamine,profoxydim, prometon, prometryn, propachlor, propanil, propaquizafop,propazine, propham, propisochlor, propoxycarbazone,propoxycarbazone-sodium, propyrisulfuron, propyzamide, prosulfocarb,pro-sulfuron, pyraclonil, pyraflufen, pyraflufen-ethyl, pyrasulfotole,pyrazolynate (pyrazolate), pyrazo-sulfuron, pyrazosulfuron-ethyl,pyrazoxyfen, pyribambenz, pyribambenz-isopropyl, pyribambenz-propyl,pyribenzoxim, pyributicarb, pyridafol, pyridate, pyriftalid,pyriminobac, pyriminobac-methyl, pyrimisulfan, pyrithiobac,pyrithiobac-sodium, pyroxasulfone, pyroxsulam, quinclorac, quinmerac,quinoclamine, quizalofop, quizalofop-ethyl, quizalofop-P,quizalofop-P-ethyl, quizalofop-P-tefuryl, rimsulfuron, saflufenacil,sethoxydim, siduron, simazine, simetryn, SL-261, sulcotrion,sulfentrazone, sulfometuron, sulfometuron-methyl, sulfosulfuron,SYN-523, SYP-249, i.e. 1-ethoxy-3-methyl-1-oxobut-3-en-2-yl5-[2-chloro-4-(trifluoromethyl)phenoxy]-2-nitrobenzoate, SYP-300, i.e.1-[7-fluoro-3-oxo-4-(prop-2-yn-1-yl)-3,4-dihydro-2H-1,4-benzoxazin-6-yl]-3-propyl-2-thioxoimidazolidine-4,5-dione,2,3,6-TBA, TCA (trichloroacetic acid), TCA-sodium, tebuthiuron,tefuryltrione, tembotrione, tepraloxydim, terbacil, terbucarb,terbumeton, terbuthylazin, terbutryn, thenylchlor, thiazopyr,thien-carbazone, thiencarbazone-methyl, thifensulfuron,thifensulfuron-methyl, thiobencarb, tiafenacil, tolpyralate,topramezone, tralkoxydim, triafamone, tri-allate, triasulfuron,triaziflam, tribenuron, tribenuron-methyl, triclopyr, trietazine,trifloxysulfuron, trifloxysulfuron-sodium, trifludimoxazin, trifluralin,triflusulfuron, triflusulfuron-methyl, tritosulfuron, urea sulfate,vernolate, XDE-848, ZJ-0862, i.e.3,4-dichloro-N-{2-[(4,6-dimethoxypyrimidin-2-yl)oxy]benzyl}aniline, andthe following compounds:

Examples for plant growth regulators are:

Acibenzolar, acibenzolar-S-methyl, 5-aminolevulinic acid, ancymidol,6-benzylaminopurine, Brassinolid, catechine, chlormequat chloride,cloprop, cyclanilide, 3-(cycloprop-1-enyl) propionic acid, daminozide,dazomet, n-decanol, dikegulac, dikegulac-sodium, endothal,endothal-dipotassium, -disodium, and -mono(N,N-dimethylalkylammonium),ethephon, flumetralin, flurenol, flurenol-butyl, flurprimidol,forchlorfenuron, gibberellic acid, inabenfide, indol-3-acetic acid(IAA), 4-indol-3-ylbutyric acid, isoprothiolane, probenazole, jasmonicacid, maleic hydrazide, mepiquat chloride, 1-methyl-cyclopropene, methyljasmonate, 2-(1-naphthyl)acetamide, 1-naphthylacetic acid,2-naphthyloxyacetic acid, nitrophenolate-mixture, paclobutrazol,N-(2-phenylethyl)-beta-alanine, N-phenylphthalamic acid, prohexadione,prohexadione-calcium, prohydrojasmone, salicylic acid, strigolactone,tecnazene, thidiazuron, triacontanol, trinexapac, trinexapac-ethyl,tsitodef, uniconazole, uniconazole-P.Methods and Uses

The compound(s) and the composition of the invention have potent plantdefense modulating potential. They can be used for controlling unwantedbacteria, in particular bacteria of the genus Xanthomonas. Thecompound(s) and the composition of the invention can be used to protectseeds, germinating seeds, emerged seedlings, plants, plant parts,fruits, harvest goods and/or the soil in which the plants grow.

Control or controlling as used herein encompasses preventive,protective, curative and eradicative treatment of unwantedmicroorganisms.

Thus, the present invention relates to a method for controllingbacterial diseases caused by bacteria of the genus Xanthomonascomprising the step of applying at least one compound of the inventionor at least one composition of the invention to the plants, plant parts,seeds, fruits or to the soil in which the plants grow.

Typically, when the compound(s) and the composition of the invention areused in curative or protective methods for controlling bacterialdiseases, an effective and plant-compatible amount thereof is applied tothe plants, plant parts, fruits, seeds or to the soil or substrates inwhich the plants grow. Suitable substrates that may be used forcultivating plants include inorganic based substrates, such as mineralwool, in particular stone wool, perlite, sand or gravel; organicsubstrates, such as peat, pine bark or sawdust; and petroleum basedsubstrates such as polymeric foams or plastic beads. Effective andplant-compatible amount means an amount that is sufficient to controlthe bacteria present or liable to appear on the cropland and that doesnot entail any appreciable symptom of phytotoxicity for said crops. Suchan amount can vary within a wide range depending on the pathogens to becontrolled, the type of crop, the crop growth stage, the climaticconditions and the respective compound(s) or composition of theinvention used. This amount can be determined by systematic field trialsthat are within the capabilities of a person skilled in the art.Diseases caused by bacterial pathogens, for example Xanthomonas species(e.g. Xanthomonas campestris pv. Oryzae), Pseudomonas species (e.g.Pseudomonas syringae pv. Lachrymans), Erwinia species (e.g. Erwiniaamylovora) may be controlled by the compounds of the present invention.The compounds of formula (I) may also be efficient for controllingphytopathogenic fungi on plants.

Plants and Plant Parts

The compound(s) and the composition of the invention may be applied toany plants or plant parts.

Plants mean all plants and plant populations, such as desired andundesired wild plants or crop plants (including naturally occurring cropplants). Crop plants may be plants which can be obtained by conventionalbreeding and optimization methods or by biotechnological and geneticengineering methods or combinations of these methods, including thegenetically modified plants (GMO or transgenic plants) and the plantcultivars which are protectable and non-protectable by plant breeders'rights.

Genetically Modified Plants (GMO)

Genetically modified plants (GMO or transgenic plants) are plants inwhich a heterologous gene has been stably integrated into the genome.The expression “heterologous gene” essentially means a gene which isprovided or assembled outside the plant and when introduced in thenuclear, chloroplastic or mitochondrial genome. This gene gives thetransformed plant new or improved agronomic or other properties byexpressing a protein or polypeptide of interest or by downregulating orsilencing other gene(s) which are present in the plant (using forexample, antisense technology, cosuppression technology, RNAinterference—RNAi—technology or microRNA—miRNA—technology). Aheterologous gene that is located in the genome is also called atransgene. A transgene that is defined by its particular location in theplant genome is called a transformation or transgenic event.

Plant cultivars are understood to mean plants which have new properties(“traits”) and have been obtained by conventional breeding, bymutagenesis or by recombinant DNA techniques. They can be cultivars,varieties, bio- or genotypes.

Plant parts are understood to mean all parts and organs of plants aboveand below the ground, such as shoots, leaves, needles, stalks, stems,flowers, fruit bodies, fruits, seeds, roots, tubers and rhizomes. Theplant parts also include harvested material and vegetative andgenerative propagation material, for example cuttings, tubers, rhizomes,slips and seeds.

Plants which may be treated in accordance with the methods of theinvention include the following: cotton, flax, grapevine, fruit,vegetables, such as Rosaceae sp. (for example pome fruits such as applesand pears, but also stone fruits such as apricots, cherries, almonds andpeaches, and soft fruits such as strawberries), Ribesioidae sp.,Juglandaceae sp., Betulaceae sp., Anacardiaceae sp., Fagaceae sp.,Moraceae sp., Oleaceae sp., Actinidaceae sp., Lauraceae sp., Musaceaesp. (for example banana trees and plantations), Rubiaceae sp. (forexample coffee), Theaceae sp., Sterculiceae sp., Rutaceae sp. (forexample lemons, oranges and grapefruit); Solanaceae sp. (for exampletomatoes), Liliaceae sp., Asteraceae sp. (for example lettuce),Umbelliferae sp., Cruciferae sp., Chenopodiaceae sp., Cucurbitaceae sp.(for example cucumber), Alliaceae sp. (for example leek, onion),Papilionaceae sp. (for example peas); major crop plants, such asGramineae sp. (for example maize, turf, cereals such as wheat, rye,rice, barley, oats, millet and triticale), Asteraceae sp. (for examplesunflower), Brassicaceae sp. (for example white cabbage, red cabbage,broccoli, cauliflower, Brussels sprouts, pak choi, kohlrabi, radishes,and oilseed rape, mustard, horseradish and cress), Fabacae sp. (forexample bean, peanuts), Papilionaceae sp. (for example soya bean),Solanaceae sp. (for example potatoes), Chenopodiaceae sp. (for examplesugar beet, fodder beet, swiss chard, beetroot); useful plants andornamental plants for gardens and wooded areas; and genetically modifiedvarieties of each of these plants.

Plants and plant cultivars which may be treated by the above disclosedmethods include plants and plant cultivars which are resistant againstone or more biotic stresses, i.e. said plants show a better defenseagainst animal and microbial pests, such as against nematodes, insects,mites, phytopathogenic fungi, bacteria, viruses and/or viroids.

Plants and plant cultivars which may be treated by the above disclosedmethods include those plants which are resistant to one or more abioticstresses. Abiotic stress conditions may include, for example, drought,cold temperature exposure, heat exposure, osmotic stress, flooding,increased soil salinity, increased mineral exposure, ozone exposure,high light exposure, limited availability of nitrogen nutrients, limitedavailability of phosphorus nutrients, shade avoidance.

Plants and plant cultivars which may be treated by the above disclosedmethods include those plants characterized by enhanced yieldcharacteristics. Increased yield in said plants may be the result of,for example, improved plant physiology, growth and development, such aswater use efficiency, water retention efficiency, improved nitrogen use,enhanced carbon assimilation, improved photosynthesis, increasedgermination efficiency and accelerated maturation. Yield may furthermorebe affected by improved plant architecture (under stress and non-stressconditions), including but not limited to, early flowering, floweringcontrol for hybrid seed production, seedling vigor, plant size,internode number and distance, root growth, seed size, fruit size, podsize, pod or ear number, seed number per pod or ear, seed mass, enhancedseed filling, reduced seed dispersal, reduced pod dehiscence and lodgingresistance.

Further yield traits include seed composition, such as carbohydratecontent and composition for example cotton or starch, protein content,oil content and composition, nutritional value, reduction inanti-nutritional compounds, improved processability and better storagestability.

Plants and plant cultivars which may be treated by the above disclosedmethods include plants and plant cultivars which are hybrid plants thatalready express the characteristic of heterosis or hybrid vigor whichresults in generally higher yield, vigor, health and resistance towardsbiotic and abiotic stresses.

Plants and plant cultivars (obtained by plant biotechnology methods suchas genetic engineering) which may be treated by the above disclosedmethods include plants and plant cultivars which are herbicide-tolerantplants, i.e. plants made tolerant to one or more given herbicides. Suchplants can be obtained either by genetic transformation, or by selectionof plants containing a mutation imparting such herbicide tolerance.

Plants and plant cultivars (obtained by plant biotechnology methods suchas genetic engineering) which may be treated by the above disclosedmethods include plants and plant cultivars which are insect-resistanttransgenic plants, i.e. plants made resistant to attack by certaintarget insects. Such plants can be obtained by genetic transformation,or by selection of plants containing a mutation imparting such insectresistance.

Plants and plant cultivars (obtained by plant biotechnology methods suchas genetic engineering) which may be treated by the above disclosedmethods include plants and plant cultivars which are disease-resistanttransgenic plants, i.e. plants made resistant to attack by certaintarget insects. Such plants can be obtained by genetic transformation,or by selection of plants containing a mutation imparting such insectresistance.

Plants and plant cultivars (obtained by plant biotechnology methods suchas genetic engineering) which may be treated by the above disclosedmethods include plants and plant cultivars which are tolerant to abioticstresses. Such plants can be obtained by genetic transformation, or byselection of plants containing a mutation imparting such stressresistance.

Plants and plant cultivars (obtained by plant biotechnology methods suchas genetic engineering) which may be treated by the above disclosedmethods include plants and plant cultivars which show altered quantity,quality and/or storage-stability of the harvested product and/or alteredproperties of specific ingredients of the harvested product.

Plants and plant cultivars (obtained by plant biotechnology methods suchas genetic engineering) which may be treated by the above disclosedmethods include plants and plant cultivars, such as cotton plants, withaltered fiber characteristics. Such plants can be obtained by genetictransformation, or by selection of plants contain a mutation impartingsuch altered fiber characteristics.

Plants and plant cultivars (obtained by plant biotechnology methods suchas genetic engineering) which may be treated by the above disclosedmethods include plants and plant cultivars, such as oilseed rape orrelated Brassica plants, with altered oil profile characteristics. Suchplants can be obtained by genetic transformation, or by selection ofplants contain a mutation imparting such altered oil profilecharacteristics.

Plants and plant cultivars (obtained by plant biotechnology methods suchas genetic engineering) which may be treated by the above disclosedmethods include plants and plant cultivars, such as oilseed rape orrelated Brassica plants, with altered seed shattering characteristics.Such plants can be obtained by genetic transformation, or by selectionof plants contain a mutation imparting such altered seed shatteringcharacteristics and include plants such as oilseed rape plants withdelayed or reduced seed shattering.

Plants and plant cultivars (obtained by plant biotechnology methods suchas genetic engineering) which may be treated by the above disclosedmethods include plants and plant cultivars, such as Tobacco plants, withaltered post-translational protein modification patterns.

Aspects of the present teaching may be further understood in light ofthe following examples, which should not be construed as limiting thescope of the present teaching in any way.

Examples Synthesis of Compounds of Formula (I) Preparation Example 1:Preparation of ethylN-[(4,5-dichloro-3-methyl-2-thienyl)carbonyl]glycinate (Compound 1.03)Step 1: Preparation of methyl3-amino-4,5-dichlorothiophene-2-carboxylate

1.35 g (5.04 mmol) of methyl3-acetamido-4,5-dichlorothiophene-2-carboxylate was dissolved in amixture of 2.1 mL (25.18 mmol) of a 37% (w/w) aqueous hydrochloric acidsolution and 8.2 mL of methanol. The mixture was heated at 75° C. for 3hours. The cooled reaction mixture was treated with a 30% (w/w) sodiumhydroxide solution at 0° C. The resulting solution was extracted withethyl acetate. Combined organic layers were dried over magnesiumsulfate, filtered and concentrated under reduced pressure to yield 812mg (98% purity, 70% yield) of methyl3-amino-4,5-dichlorothiophene-2-carboxylate as a brown solid used assuch in the next step. Log P=3.11. (M+H)=226.

Step 2: Preparation of methyl3-bromo-4,5-dichlorothiophene-2-carboxylate

To a solution of 763 mg (3.41 mmol) of copper bromide (II) and 0.53 mL(90% purity, 3.99 mmol) of tert-butyl nitrite in 10.5 mL of anhydrousacetonitrile was added portion wise 600 mg (88% purity, 2.33 mmol) ofmethyl 3-amino-4,5-dichlorothiophene-2-carboxylate at 0° C. After gasevolved, the solution was stirred at room temperature for 18 hours. Thereaction mixture was diluted with ethyl acetate and acidified with a 1 Maqueous hydrochloric acid solution. The aqueous layer was extractedthree times with ethyl acetate. Combined organic layers were dried overmagnesium sulfate, filtered and concentrated under reduced pressure. Theresidue was purified by column chromatography on silica gel (gradientn-heptane/ethyl acetate) to yield 563 mg (98% purity, 82% yield) ofmethyl 3-bromo-4,5-dichlorothiophene-2-carboxylate as a yellow solid.Log P=3.99. (M+H)=288.

Step 3: Preparation of 3-bromo-4,5-dichlorothiophene-2-carboxylic acid(Compound VIIIa.03)

To a solution of 250 mg (0.86 mmol) of methyl3-bromo-4,5-dichlorothiophene-2-carboxylate in 5 mL of tetrahydrofuranwas added dropwise 1 mL of a 1.9 M aqueous potassium hydroxide solution(1.9 mmol). The reaction was stirred at room temperature for 18 hours.The reaction mixture was diluted with ethyl acetate, water and asaturated aqueous sodium bicarbonate solution. The organic layer waswashed twice with a saturated aqueous sodium bicarbonate solution.Combined aqueous layers were carefully acidified with a 37% (w/w)aqueous hydrochloric acid solution at 0° C. and extracted with ethylacetate. Combined organic layers were dried over magnesium sulfate,filtered and concentrated under reduced pressure to yield 219 mg (96%purity, 88% yield) of 3-bromo-4,5-dichlorothiophene-2-carboxylic acid asa white solid. Log P=2.51. (M−H)=273.

Step 4: Preparation of ethylN-[(3-bromo-4,5-dichloro-2-thienyl)carbonyl]glycinate (Compound VIa.01)

In a 5 mL microwave vial under inert atmosphere, a solution of 157 mg(0.93 mmol) of 2-chloro-1,3-dimethylimidazolidinium chloride dissolvedin 3 mL of dichloromethane was added over a solution of 197 mg (0.72mmol) of 3-bromo-4,5-dichlorothiophene-2-carboxylic acid and 0.54ml_(3.07 mmol) of N,N-diisopropylethylamine dissolved in 7 mL ofdichloromethane. After 5 min of stirring, 200 mg (1.43 mmol) of ethylglycinate hydrochloride (1:1) was added and the reaction mixture wasstirred at room temperature for 20 hours. The reaction mixture wasquenched with water and extracted with dichloromethane. Combined organiclayers were dried over magnesium sulfate, filtered and concentratedunder reduced pressure. The residue was purified by columnchromatography on silica gel (gradient n-heptane/ethyl acetate) to yield209 mg (100% purity, 81% yield) of ethylN-[(3-bromo-4,5-dichloro-2-thienyl)carbonyl]glycinate as a white solid.Log P=3.33. (M+H)=360.

Step 5: Preparation of ethylN-[(4,5-dichloro-3-methyl-2-thienyl)carbonyl]glycinate (Compound 1.03)

In a 5 mL microwave vial under inert atmosphere, 100 mg (0.27 mmol) ofethyl N-[(3-bromo-4,5-dichloro-2-thienyl)carbonyl]glycinate, 25 mg (0.41mmol) of methylboronic acid, 3.1 mg (0.01 mmol) of palladium(II)acetate, 7.8 mg (0.02 mmol) of tricyclohexylphosphine and 206 mg (0.96mmol) of potassium phosphate tribasic were successively added followedby degassed toluene (1.25 mL) and water (0.13 mL). The vial was sealedand the reaction mixture was stirred at 100° C. for 18 hours. Thereaction mixture was diluted with water and extracted withdichloromethane. Combined organic layers were filtered through a ChemElut™ cartridge and concentrated under reduced pressure. The residue waspurified by preparative high performance liquid chromatography (gradientacetonitrile/aqueous solution of formic acid (1%)) to yield 38 mg (100%purity, 46% yield) of ethylN-[(4,5-dichloro-3-methyl-2-thienyl)carbonyl]glycinate as a white solid.Log P=2.95. (M+H)=296.

Preparation Example 2: Preparation of ethylN-[(4,5-dibromo-3-methyl-2-thienyl)carbonyl]-valinate (Compound 1.04)

To a solution of 154 mg (0.50 mmol) of4,5-dibromo-3-methylthiophene-2-carboxylic acid and 183 mg (1.00 mmol)of DL-valine ethyl ester hydrochloride dissolved in 3 mL oftetrahydrofuran was added 0.21 mL (1.51 mmol) of triethylamine followedby 0.45 mL (0.75 mmol) of a 50% (w/w) propanephosphonic anhydridesolution in ethyl acetate. The reaction mixture was stirred at roomtemperature for 2 hours. The reaction mixture was quenched with asaturated aqueous solution of sodium bicarbonate and extracted withethyl acetate. Combined organic layers were dried over magnesiumsulfate, filtered and concentrated under reduced pressure. The residuewas purified by column chromatography on silica gel (gradientn-heptane/ethyl acetate) to yield 103 mg (95% purity, 45% yield) ofethyl N-[(4,5-dibromo-3-methyl-2-thienyl)carbonyl]-valinate as a whitesolid. Log P=4.32. (M+H)=426.

Preparation Example 3: Preparation ofN-[(4,5-dibromo-3-methyl-2-thienyl)carbonyl]-valine (Compound 1.07)

To a solution of 164 mg (0.38 mmol) of ethylN-[(4,5-dibromo-3-methyl-2-thienyl)carbonyl]-valinate and in 3 mL oftetrahydrofuran was added dropwise 0.81 mL of a 1 M lithium hydroxidesolution (0.81 mmol). The reaction was stirred at room temperature for18 hours. The reaction mixture was diluted with ethyl acetate and asaturated aqueous sodium bicarbonate solution. The organic layer waswashed twice with a saturated aqueous sodium bicarbonate solution.Combined aqueous layers were carefully acidified with a 37% (w/w)aqueous hydrochloric acid solution at 0° C. and extracted with ethylacetate. Combined organic layers were dried over magnesium sulfate,filtered and concentrated under reduced pressure to yield 151 mg (98%purity, 96% yield) ofN-[(4,5-dibromo-3-methyl-2-thienyl)carbonyl]-valine as a white solid.Log P=2.92. (M+H)=398.

Preparation Example 4: Preparation of ethyl1-{[(4,5-dibromo-3-methyl-2-thienyl)carbonyl]amino}cyclopropanecarboxylate(Compound I.01)

To a solution of 200 mg (0.60 mmol) of ethyl1-{[(4-bromo-3-methyl-2-thienyl)carbonyl]amino}cyclopropanecarboxylate(compound IXa.01) in 6 mL of anhydrous N,N-dimethylformamide was added129 mg (0.72 mmol) of N-bromosuccinimide. The reaction was stirred at50° C. for 18 hours. The reaction mixture was partitioned between ethylacetate and water and extracted with ethyl acetate. Combined organiclayers were filtered through a Chem Elut™ cartridge and concentratedunder reduced pressure. The residue was purified by preparative highperformance liquid chromatography (gradient acetonitrile/aqueoussolution of formic acid (1%)) to yield 148 mg (100% purity, 60% yield)of ethyl1-{[(4,5-dibromo-3-methyl-2-thienyl)carbonyl]amino}cyclopropanecarboxylateas a white solid. Log P=3.22. (M+H)=410.

Preparation Example 5: Preparation of ethyl1-{[(4,5-dibromo-3-methyl-2-thienyl)carbonyl]amino}cyclopropanecarboxylate(Compound I.01) Step 1: Preparation of ethyl1-[({4-bromo-5-[(tert-butoxycarbonyl)amino]-3-methyl-2-thienyl}carbonyl)amino]cyclopropanecarboxylate(Compound XIa.01)

To a solution of 92 mg (0.27 mmol) of4-bromo-5-[(tert-butoxycarbonyl)amino]-3-methylthiophene-2-carboxylicacid (compound XIIIa.02) and 67 mg (0.41 mmol) of ethyl1-aminocyclopropanecarboxylate hydrochloride dissolved in 1.4 mL ofdichloromethane was added 0.14 mL (0.82 mmol) ofN,N-diisopropylethylamine followed by 135 mg (0.35 mmol) of1-[bis(dimethylamino)methylene]-1H-1,2,3-triazolo[4,5-b]pyridinium3-oxid hexafluorophosphate. The reaction mixture was stirred at roomtemperature for 3.5 hours. The reaction mixture was quenched with waterand extracted with dichloromethane. Combined organic layers werefiltered through a Chem Elut™ cartridge and concentrated under reducedpressure. The residue was purified by column chromatography on silicagel (gradient n-heptane/ethyl acetate) to yield 95 mg (93% purity, 72%yield) of ethyl1-[({4-bromo-5-[(tert-butoxycarbonyl)amino]-3-methyl-2-thienyl}carbonyl)amino]cyclopropanecarboxylateas an orange solid. Log P=3.28. (M+H)=447.

Step 2: Preparation of ethyl1-{[(5-amino-4-bromo-3-methyl-2-thienyl)carbonyl]amino}cyclopropanecarboxylate(Compound Xa.01)

To a solution of 60 mg (0.13 mmol) of1-[(tert-butoxycarbonyl)amino]-3-methyl-2-thienyl)carbonyl)amino]cyclopropanecarboxylatein 0.60 mL of chloroform was added 0.62 mL of trifluoroacetic acid. Thereaction was stirred at room temperature for 18 hours. The reactionmixture was diluted with toluene and concentrated under reducedpressure. The residue was purified by preparative high performanceliquid chromatography (gradient acetonitrile/aqueous solution ofammonium acetate (1 mM)) to yield 35 mg (100% purity, 74% yield) ofethyl1-{[(5-amino-4-bromo-3-methyl-2-thienyl)carbonyl]amino}cyclopropanecarboxylateas a white solid. Log P=1.92. (M+H)=347.

Step 3: Preparation of ethyl1-{[(4,5-dibromo-3-methyl-2-thienyl)carbonyl]amino}cyclopropanecarboxylate(Compound I.01)

To a solution of copper(II) bromide (28.9 mg, 0.13 mmol) in 0.5 mL ofanhydrous acetonitrile was added dropwise tert-butyl nitrite (17 μL,0.13 mmol) at 0° C. The reaction mixture was allowed to warm to roomtemperature before dropwise addition of a solution of 30 mg (0.08 mmol)of ethyl1-{[(5-amino-4-bromo-3-methyl-2-thienyl)carbonyl]amino}cyclopropanecarboxylatein 0.7 mL of anhydrous acetonitrile. The reaction mixture was stirred atroom temperature for 2 hours. The reaction mixture was diluted withethyl acetate and carefully acidified with a 1 M aqueous hydrochloricacid solution. The aqueous layer was extracted three times with ethylacetate. Combined organic layers were dried over magnesium sulfate,filtered and concentrated under reduced pressure. The residue waspurified column chromatography on silica gel (gradient n-heptane/ethylacetate) to yield 11 mg (100% purity, 31% yield) of ethyl1-{[(4,5-dibromo-3-methyl-2-thienyl)carbonyl]amino}cyclopropanecarboxylateas a white solid. Log P=3.19. (M+H)=410.

Exemplary Compounds

The exemplary compounds according to the invention as shown in tablesI.1, I.2, I.3, I.4, I.5, I.6 and I.7 were prepared in analogy with theexamples provided above and/or in accordance with the generaldescription of the processes herein disclosed. The exemplary compoundsare racemic unless specified differently.

The following table I.1 illustrates in a non-limiting manner examples ofcompounds according to formula (I).

TABLE I.1 Ex. No R¹ R² R³ R⁴ R⁵ R⁶ LogP Enantiomer Optical Rotation*I.01 Br Br Me —CH₂—CH₂— Et 3.19^([a]) I.02 Br Br Me H H Et 3.02^([a])I.03 Cl Cl Me H H Et 2.90^([a]) I.04 Br Br Me isopropyl H Et 4.32^([a])I.05 Br Br Me 2-methylpropyl H Et 4.56^([a]) I.06 Br Br Me —CH₂—CH₂— H2.25^([a]) I.07 Br Br Me isopropyl H H 2.92^([a]) I.08 Br Br Mepropan-2-yl H Et 4.32^([a]) (S) +22.1° (c = 0.99, CH2Cl2, 20° C.) I.09Br Br Me H H Me 2.64^([a]) I.10 Br Br Me H H H 2.05^([a]) I.11 Br Br Mepropan-2-yl H Me 3.87^([a]) (S) +3.6° (c = 1.13, MeOH, 25° C.) I.12 BrBr Me isopropyl H (Z)-hex-3-en-1-yl 5.75^([a]) I.13 Br Br Me isopropyl Hprop-2-yn-1-yl 4.06^([a]) I.14 Br Br Me isopropyl H 2-methylpropyl5.22^([a]) I.15 Br Br Me isopropyl H cyanomethyl 3.69^([a]) I.16 Br BrMe isopropyl H oxetan-3-yl 3.58^([a]) I.17 Br Br Me isopropyl Hthietan-3-yl 4.67^([a]) I.18 Br Br Me isopropyl H 1,1-dioxothietan-3-yl3.42^([a]) I.19 Br Br Me isopropyl H oxolan-3-yl 3.78^([a]) I.20 Br BrMe isopropyl H trimethylsilylmethyl 5.78^([a]) I.21 Br Br Me Me H Et3.39^([a]) I.22 Br Br Me butan-2-yl H Me 4.30^([a]) (2S, 3S) I.23 Br BrMe (4-hydroxyphenyl)methyl H Et 3.33^([a]) I.24 Cl Cl Me2-methylsulfanylethyl H Et 3.94^([a]) (S) +26.4° (c = 1.06, CDCl3, 25°C.) I.25 Cl Cl Me isopropyl H Et 4.23^([a]) (S) +44.7° (c = 1.08, CDCl3,25° C.) I.26 Cl Cl Me benzyl H Et 4.46^([a]) (S) +91° (c = 1.06, CDCl3,25° C.) I.27 Cl Cl Me Me H Et 3.31^([a]) I.28 Cl Cl Me H H tert-butyl3.77^([a]) I.29 Cl Cl Me isopropyl H Me 3.79^([a]) (S) +40° (c = 1,CDCl3, 25° C.) I.30 Cl Cl Me 2-methylsulfanylethyl H Me 3.55^([a]) (S)+30.8° (c = 1.04, CDCl3, 25° C.) I.31 Cl Cl Me H H Me 2.51^([a]) I.32 ClCl Me butan-2-yl H Me 4.23^([a]) (2S, 3S) +46.9° (c = 1.07, CDCl3, 25°C.) I.33 Cl Cl Me 2-methylpropyl H Et 4.54^([a]) (S) +29.4° (c = 1.02,CDCl3, 25° C.) I.34 Cl Cl Me H H benzyl 3.76^([a]) I.35 Cl Cl Me2-methylsulfanylethyl H Me 3.55^([a]) I.36 Cl Cl Me2-methylsulfanylethyl H Me 3.55^([a]) (R) I.37 Cl Cl Me 2-methylpropyl HEt 4.51^([a]) I.38 Cl Cl Me benzyl H Et 4.46^([a]) I.39 Cl Cl Me(4-hydroxyphenyl)methyl H Et 3.29^([a]) I.40 Cl Cl Me isopropyl H Et4.23^([a]) I.41 Cl Cl Me H H isopropyl 3.29^([a]) I.42 Cl Cl Me Me H Et3.31^([a]) (R) I.43 Cl Cl Me —CH₂—CH₂— Et 3.08^([a]) I.44 Cl Cl Meisopropyl H Et 4.23^([a]) (R) −48.4° (c = 1.08, CDCl3, 25° C.) I.45 ClCl Me benzyl H Et 4.46^([a]) (R) −91.2° (c = 1.08, CDCl3, 25° C.) I.46Cl Cl Me isopropyl H Me 3.79^([a]) (R) I.47 Cl Cl Me2-methylsulfanylethyl H Et 3.94^([a]) I.48 Cl Cl Me H H propyl3.35^([a]) I.49 Br Br Me isopropyl H isopropyl 4.77^([a]) I.50 Cl Cl Me—CH₂—CH₂— Me 2.75^([a]) I.51 Cl Cl Me —CH₂—CH₂— H 2.26^([a]) I.52 Br BrMe isopropyl H cyclopropylmethyl 4.80^([a]) I.53 Br Br Me isopropyl Hcyclobutyl 4.98^([a]) I.54 Br Br Me isopropyl H propyl 4.77^([a]) I.55Br Br Me isopropyl H butyl 5.25^([a]) I.56 Br Br Me isopropyl Hcyclopropyl 4.37^([a]) I.57 Br Br Me isopropyl H benzyl 5.03^([a]) I.58Br Br Me isopropyl H allyl 4.46^([a]) I.59 Br Br Me isopropyl H2,2,2-trifluoroethyl 4.51^([a]) I.60 Br Br Me isopropyl H phenyl4.85^([a]) I.61 Br Br Me isopropyl H tert-butyl 5.25^([a]) I.62 Br Br Mepropan-2-yl H Et 4.37^([a]) (R) −44.4° (c = 1.04, CDCl3, 25° C.) I.63 BrBr Me propan-2-yl H Me 3.91^([a]) (R) I.64 Br Br Me isopropyl H Me3.91^([a]) I.65 Br Br Me benzyl H Et 4.59^([a]) (R) −64.1° (c = 1.41,CDCl3, 25° C.) I.66 Br Br Me benzyl H Et 4.59^([a]) (S) +58° (c = 1,CDCl3, 25° C.) I.67 Br Br Me benzyl H Et 4.59^([a]) I.68 Br Br Me2-methylpropyl H Et 4.66^([a]) (R) −28° (c = 1, CDCl3, 25° C.) I.69 BrBr Me 2-methylpropyl H Et 4.66^([a]) (S) +26° (c = 1, CDCl3, 25° C.)I.70 Br Br Me 2-methylsulfanylethyl H Me 3.69^([a]) (R) I.71 Br Br Me2-methylsulfanylethyl H Me 3.69^([a]) (S) +26° (c = 1, CDCl3, 25° C.)I.72 Br Br Me 2-methylsulfanylethyl H Me 3.69^([a]) I.73 Cl Cl Me benzylH Me 4.12^([a]) (S) I.74 Cl Cl Me 2-methylpropyl H Et 4.59^([a]) (R)I.75 Cl Cl Me phenyl H Et 4.37^([a]) I.76 Br Br Me phenyl H Et4.44^([a]) I.77 Br Br Me H H oxan-4-yl 2.86^([a]) I.78 Br Br Me H Hisopropyl 3.40^([a]) I.79 Br Br Me Me H H 2.39^([a]) I.80 Cl Cl Me H H H2.05^([a]) I.81 Cl Cl Me Me H H 2.28^([a]) I.82 Cl Cl Me isopropyl H H2.96^([a]) I.83 Cl Cl Me butan-2-yl H H 3.31^([a]) (2S, 3S) +12.9° C. (c= 1.4, DMSO, 25° C.) I.84 Cl Cl Me 2-methylpropyl H H 3.31^([a]) I.85 ClCl Me 2-methylsulfanylethyl H H 2.80^([a]) I.86 Cl Cl Me benzyl H H3.31^([a]) I.87 Br Br Me 2-methylsulfanylethyl H H 2.89^([a]) I.88 Br BrMe benzyl H H 3.30^([a]) I.89 Br Br Me butan-2-yl H H 3.37^([a]) (2S,3S) +14.3° (c = 1.40, MeOH, 20° C.) I.90 Br Br Me 2-methylpropyl H H3.34^([a]) I.91 Cl Cl Me isopropyl H Me 4.34^([a]) I.92 Br Br Me—CH₂—CH₂— Me 2.86^([a]) Note: Me: methyl, Et: ethyl *Optical rotation:concentration c is expressed in g/100 mL

The following table I.2 illustrates in a non-limiting manner examples ofintermediates according to formula (IVa).

TABLE I.2 Ex No R¹ R² R³ U^(1a) LogP IVa.01 Br Br Me 2-methylpropoxy6.12^([a]) IVa.02 Cl Cl Me OEt 4.80^([a]) IVa.03 Cl Cl Me2-methylpropoxy 6.05^([a]) Note: Me: methyl, Et: ethyl

The following table I.3 illustrates in a non-limiting manner examples ofintermediates according to formula (Via).

TABLE I.3 Ex No R¹ R² R⁴ R⁵ R⁶ U^(2a) LogP VIa.01 Cl Cl H H Et Br3.33^([a]) VIa.02 Cl Cl H H Me I 2.90^([a]) VIa.03 Br Br H H Me I2.96^([a]) VIa.04 Cl Cl —CH₂—CH₂— Et Br 3.45^([a]) VIa.05 Cl Cl—CH₂—CH₂— Et I 3.39^([a]) VIa.06 Cl Cl —CH₂—CH₂— H I 2.34^([a]) VIa.07Br Br —CH₂—CH₂— Et I 3.41^([a]) VIa.08 Br Br —CH₂—CH₂— Me I 3.06^([a])VIa.09 Br Br —CH₂—CH₂— H I 2.43^([a]) VIa.10 Br Br H H Et I 3.35^([a])VIa.11 Br Br isopropyl H Et I 4.78^([a]) VIa.12 Cl Cl H H Et I3.31^([a]) VIa.13 Cl Cl H H H I 2.21^([a]) VIa.14 Br Br benzyl H Et I4.93^([a]) VIa.15 Br Br 2-methylpropyl H Et I 5.01^([a]) VIa.16 Br Br2-methylsulfanylethyl H Et I 4.37^([a]) VIa.17 Cl Cl isopropyl H Et Br4.88^([a]) VIa.18 Cl Cl 2-methylpropyl H Et Br 5.17^([a]) VIa.19 Cl Cl2-methylsulfanylethyl H Et Br 4.46^([a]) VIa.20 Cl Cl benzyl H Et Br5.01^([a]) VIa.21 Cl Cl isopropyl H Et I 4.85^([a]) VIa.22 Cl Cl2-methylpropyl H Et I 5.08^([a]) VIa.23 Cl Cl 2-methylsulfanylethyl H EtI 4.40^([a]) VIa.24 Cl Cl benzyl H Et I 5.00^([a]) Note: Me: methyl, Et:ethyl

The following table I.4 illustrates in a non-limiting manner examples ofintermediates according to formula (Villa).

TABLE I.4 Ex No R¹ R² U^(2a) U^(1a) LogP VIIIa.01 Cl Cl I OEt 4.73^([b])VIIIa.02 Cl Cl Br OMe 4.11^([a]) VIIIa.03 Cl Cl Br OH 2.52^([a])VIIIa.04 Br Br I OMe 4.20^([a]) VIIIa.05 Cl Cl I OMe 4.15^([a]) VIIIa.06Cl Cl I OH 2.64^([a]) VIIIa.07 Br Br I OEt 4.78^([a]) VIIIa.08 Cl Cl BrOEt 4.58^([a]) Note: Me: methyl, Et: ethyl

The following table I.5 illustrates in a non-limiting manner examples ofintermediates according to formula (IXa) and (IXb).

TABLE I.5 Ex No R³ R⁴ R⁵ R⁶ U^(4a) U^(5a) LogP IXa.01 Me —CH₂—CH₂— Et Br2.57^([a]) IXa.02 Me H H Et Br 2.39^([a]) IXa.03 Me isopropyl H Et Br3.65^([a]) IXa.04 Me benzyl H Et Br 3.90^([a]) IXb.01 Me —CH₂—CH₂— Et Br2.49^([a]) Note: Me: methyl, Et: ethyl

The following table I.6 illustrates in a non-limiting manner examples ofintermediates according to formula (Xa) and (XIa).

TABLE I.6 Ex No R² R³ R⁴ R⁵ R⁶ V LogP Xa.01 Br Me —CH₂—CH₂— Et1.97^([a]) XIa.01 Br Me —CH₂—CH₂— Et tert-butoxycarbonyl 3.44^([b])Note: Me: methyl, Et: ethyl

The following table I.7 illustrates in a non-limiting manner examples ofintermediates according to formula (XIIIa).

TABLE I.7 Ex No R² R³ U^(1a) V LogP XIIIa.01 Br Me OEttert-butoxycarbonyl 4.62^([a]) XIIIa.02 Br Me OH tert-butoxycarbonyl2.86^([a]) Note: Me: methyl, Et: ethyl

In the above tables, measurement of Log P values was performed accordingto EEC directive 79/831 Annex V.A8 by HPLC (High Performance LiquidChromatography) on reversed phase columns with the following methods:

-   -   ^([a]) Log P value is determined by measurement of LC-UV, in an        acidic range, with 0.1% formic acid in water and acetonitrile as        eluent (linear gradient from 10% acetonitrile to 95%        acetonitrile).    -   ^([b]) Log P value is determined by measurement of LC-UV, in a        neutral range, with 0.001 molar ammonium acetate solution in        water and acetonitrile as eluent (linear gradient from 10%        acetonitrile to 95% acetonitrile).    -   ^([c]) Log P value is determined by measurement of LC-UV, in an        acidic range, with 0.1% phosphoric acid and acetonitrile as        eluent (linear gradient from 10% acetonitrile to 95%        acetonitrile).

If more than one Log P value is available within the same method, allthe values are given and separated by “+”.

Calibration was done with straight-chain alkan2-ones (with 3 to 16carbon atoms) with known Log P values (measurement of Log P values usingretention times with linear interpolation between successive alkanones).Lambda-max-values were determined using UV-spectra from 200 nm to 400 nmand the peak values of the chromatographic signals.

NMR-Peak Lists

Table A provides the NMR data (¹H) of some compounds disclosed in theabove tables.

1H-NMR data of selected examples are written in form of 1H-NMR-peaklists. To each signal peak are listed the 8-value in ppm and the signalintensity in round brackets. Between the δ-value—signal intensity pairsare semicolons as delimiters.

The peak list of an example has therefore the form:

δ₁ (intensity₁); δ₂ (intensity₂); . . . ; δ_(i) (intensity_(i)); . . . ;δ_(n) (intensity_(n))

Intensity of sharp signals correlates with the height of the signals ina printed example of a NMR spectrum in cm and shows the real relationsof signal intensities. From broad signals, several peaks or the middleof the signal and their relative intensity in comparison to the mostintensive signal in the spectrum can be shown.

For calibrating chemical shift for 1H spectra, we use tetramethylsilaneand/or the chemical shift of the solvent used, especially in the case ofspectra measured in DMSO. Therefore, in NMR peak lists,tetramethylsilane peak can occur but not necessarily.

The 1H-NMR peak lists are similar to classical 1H-NMR prints andcontains therefore usually all peaks, which are listed at classicalNMR-interpretation.

Additionally they can show like classical 1H-NMR prints signals ofsolvents, stereoisomers of the target compounds, which are also objectof the invention, and/or peaks of impurities.

To show compound signals in the delta-range of solvents and/or water theusual peaks of solvents, for example peaks of DMSO in DMSO-D6 and thepeak of water are shown in our 1H-NMR peak lists and have usually onaverage a high intensity.

The peaks of stereoisomers of the target compounds and/or peaks ofimpurities have usually on average a lower intensity than the peaks oftarget compounds (for example with a purity >90%).

Such stereoisomers and/or impurities can be typical for the specificpreparation process. Therefore, their peaks can help to recognize thereproduction of our preparation process via“side-products-fingerprints”.

An expert, who calculates the peaks of the target compounds with knownmethods (MestreC, ACD-simulation, but also with empirically evaluatedexpectation values) can isolate the peaks of the target compounds asneeded optionally using additional intensity filters. This isolationwould be similar to relevant peak picking at classical 1H-NMRinterpretation.

Further details of NMR-data description with peak lists you find in thepublication “Citation of NMR Peaklist Data within Patent Applications”of the Research Disclosure Database Number 564025.

TABLE A NMR peak lists I.01: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.2983 (5.4);6.3048 (1.0); 4.2377 (1.2); 4.2139 (3.8); 4.1901 (3.8); 4.1664 (1.2);2.5728 (16.0); 1.7079 (1.0); 1.6912 (2.9); 1.6804 (3.0); 1.6651 (1.3);1.6024 (1.2); 1.3339 (1.3); 1.3188 (3.0); 1.3079 (3.1); 1.2970 (4.3);1.2912 (1.6); 1.2732 (8.2); 1.2495 (3.9); 0.0356 (6.8) I.02:¹H-NMR(300.2 MHz, CDCl3): δ = 7.2987 (2.8); 6.3702 (0.5); 5.3358 (1.0);4.3360 (1.1); 4.3122 (3.4); 4.2884 (3.5); 4.2646 (1.2); 4.2258 (4.6);4.2093 (4.5); 2.5934 (16.0); 1.6227 (3.3); 1.3760 (4.2); 1.3522 (8.4);1.3284 (4.0); 0.0353 (3.4) I.03: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.6720(0.4); 8.6579 (0.9); 8.6436 (0.4); 4.1518 (1.3); 4.1340 (4.0); 4.1163(4.0); 4.0985 (1.3); 3.9757 (3.9); 3.9610 (3.9); 3.3498 (56.9); 2.5264(0.4); 2.5215 (0.6); 2.5129 (6.9); 2.5085 (13.6); 2.5040 (17.5); 2.4994(12.6); 2.4949 (6.0); 2.4038 (16.0); 1.2386 (0.4); 1.2239 (4.5); 1.2061(9.2); 1.1883 (4.4) I.04: ¹H-NMR(499.9 MHz, d₆-DMSO): δ = 8.5246 (2.1);8.5091 (2.1); 4.2262 (2.0); 4.2121 (2.9); 4.2044 (0.6); 4.1971 (2.1);4.1901 (1.4); 4.1827 (0.9); 4.1759 (1.4); 4.1684 (2.7); 4.1617 (0.5);4.1542 (2.7); 4.1448 (0.9); 4.1400 (0.9); 4.1306 (2.7); 4.1231 (0.5);4.1164 (2.7); 4.1089 (1.4); 4.1023 (0.9); 4.0947 (1.4); 4.0805 (0.4);3.3228 (2.7); 2.5144 (1.0); 2.5109 (2.1); 2.5073 (2.8); 2.5037 (2.0);2.5002 (0.9); 2.4121 (26.4); 2.1959 (0.3); 2.1822 (1.0); 2.1686 (1.8);2.1550 (1.8); 2.1414 (1.1); 2.1278 (0.4); 1.2263 (7.8); 1.2120 (16.0);1.1978 (7.7); 0.9722 (10.8); 0.9585 (11.5); 0.9537 (11.5); 0.9401 (10.5)I.05: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.2984 (1.5); 6.3390 (0.7); 6.3132(0.9); 4.8070 (0.6); 4.7792 (1.2); 4.7623 (0.9); 4.7517 (0.7); 4.7355(0.5); 4.2892 (1.4); 4.2654 (4.3); 4.2417 (4.4); 4.2179 (1.5); 2.5719(4.2); 2.5621 (16.0); 1.7908 (0.9); 1.7725 (1.3); 1.7611 (1.3); 1.7538(1.5); 1.7462 (1.9); 1.7253 (1.4); 1.7062 (0.9); 1.6863 (1.3); 1.6608(1.0); 1.6564 (1.0); 1.6324 (0.7); 1.4570 (1.0); 1.3543 (5.0); 1.3305(10.0); 1.3067 (5.1); 1.2917 (1.0); 1.2857 (1.0); 1.0435 (0.3); 1.0202(6.9); 1.0065 (10.3); 0.9871 (6.6); 0.9283 (0.3); 0.9064 (0.7); 0.8832(0.4); 0.0297 (0.4); 0.0254 (0.7) I.06: ¹H-NMR(499.9 MHz, d₆-DMSO): δ =12.4961 (2.0); 8.7878 (13.5); 3.3226 (11.2); 2.5437 (0.5); 2.5119(15.4); 2.5084 (22.0); 2.5049 (17.8); 2.4800 (0.4); 2.4158 (70.6);2.2841 (0.4); 2.0928 (6.3); 1.4392 (0.4); 1.4307 (0.4); 1.4239 (0.5);1.4083 (5.6); 1.3989 (14.1); 1.3924 (16.0); 1.3839 (6.4); 1.3521 (0.6);1.3056 (0.4); 1.2658 (0.7); 1.2420 (3.2); 1.2155 (0.4); 1.2021 (0.4);1.1883 (0.6); 1.1763 (0.6); 1.1716 (0.8); 1.1622 (0.6); 1.1572 (1.2);1.1482 (0.7); 1.1433 (0.7); 1.1222 (6.5); 1.1135 (14.8); 1.1070 (15.3);1.0976 (5.6); 1.0670 (0.4); 0.8609 (0.5) I.07: ¹H-NMR(499.9 MHz,d₆-DMSO): δ = 12.7425 (0.4); 8.3639 (2.1); 8.3478 (2.1); 4.2207 (2.0);4.2080 (2.3); 4.2047 (2.2); 4.1920 (2.0); 3.5752 (2.1); 3.3269 (0.8);2.5162 (1.6); 2.5125 (2.7); 2.5088 (3.6); 2.5052 (2.5); 2.5016 (1.1);2.4179 (28.8); 2.2015 (0.3); 2.1880 (1.0); 2.1745 (1.6); 2.1612 (1.6);2.1477 (1.0); 2.1342 (0.3); 0.9629 (16.0); 0.9494 (15.5) I.08:¹H-NMR(499.9 MHz, d₆-DMSO): δ = 8.5386 (2.0); 8.5233 (2.0); 4.2147(2.1); 4.2001 (3.4); 4.1854 (3.2); 4.1777 (1.0); 4.1709 (1.5); 4.1635(2.7); 4.1567 (0.6); 4.1493 (2.7); 4.1398 (1.0); 4.1351 (1.0); 4.1257(2.7); 4.1182 (0.6); 4.1115 (2.6); 4.1040 (1.4); 4.0973 (0.9); 4.0898(1.3); 4.0756 (0.4); 3.3185 (58.2); 2.5358 (0.4); 2.5125 (2.9); 2.5090(5.5); 2.5054 (7.2); 2.5018 (5.0); 2.4983 (2.3); 2.4080 (27.6); 2.1877(0.4); 2.1741 (1.1); 2.1605 (1.8); 2.1469 (1.8); 2.1333 (1.1); 2.1197(0.4); 1.2360 (0.5); 1.2208 (8.0); 1.2065 (16.0); 1.1923 (7.5); 0.9677(11.8); 0.9540 (12.5); 0.9494 (11.9); 0.9357 (10.5) I.09: ¹H-NMR(300.2MHz, CDCl3): δ = 7.2988 (3.8); 6.3470 (0.4); 4.2461 (4.5); 4.2294 (4.4);3.8469 (14.9); 2.5954 (16.0); 1.6069 (3.2); 0.0363 (4.7) I.10:¹H-NMR(499.9 MHz, d6-DMSO): δ = 12.6968 (0.6); 8.5442 (2.2); 8.5326(4.3); 8.5209 (2.3); 3.8971 (15.9); 3.8854 (16.0); 3.3973 (0.4); 3.3833(0.6); 3.3296 (14.9); 2.5810 (0.5); 2.5466 (0.4); 2.5207 (9.4); 2.5166(4.5); 2.5129 (8.3); 2.5093 (11.3); 2.5056 (8.3); 2.5020 (4.1); 2.4530(64.6); 2.3213 (0.3) I.11: ¹H-NMR(400.1 MHz, d₆-DMSO): δ = 8.5820 (1.4);8.5628 (1.4); 4.2506 (1.2); 4.2323 (2.1); 4.2141 (1.3); 3.6755 (16.0);3.3300 (2.1); 2.5111 (1.7); 2.5071 (1.4); 2.4136 (15.3); 2.1826 (0.6);2.1656 (1.1); 2.1486 (1.2); 2.1316 (0.7); 0.9701 (6.7); 0.9531 (7.3);0.9458 (7.6); 0.9287 (6.8) I.12: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.2989(1.9); 6.3630 (0.6); 6.3356 (0.6); 5.5734 (0.5); 5.5680 (0.4); 5.5618(0.4); 5.5427 (0.5); 5.5375 (0.7); 5.5331 (0.4); 5.5134 (0.4); 5.3759(0.4); 5.3567 (0.4); 5.3518 (0.7); 5.3465 (0.5); 5.3278 (0.4); 5.3216(0.4); 5.3160 (0.5); 4.7510 (1.2); 4.7362 (1.2); 4.7229 (1.2); 4.7082(1.2); 4.2548 (0.5); 4.2426 (0.9); 4.2197 (2.5); 4.1976 (2.5); 4.1753(0.9); 4.1626 (0.5); 2.6800 (0.3); 2.5914 (16.0); 2.4882 (0.6); 2.4650(1.6); 2.4419 (1.6); 2.4304 (0.4); 2.4199 (0.6); 2.3411 (0.4); 2.3347(0.5); 2.3197 (0.5); 2.3116 (0.6); 2.2967 (0.6); 2.2887 (0.5); 2.2738(0.5); 2.1186 (1.0); 2.1163 (1.0); 2.0919 (1.6); 2.0674 (1.1); 2.0652(1.1); 1.0424 (6.3); 1.0322 (4.4); 1.0195 (6.3); 1.0066 (12.2); 0.9822(9.5); 0.0339 (2.3) I.13: ¹H-NMR(499.9 MHz, CDCl3): δ = 7.2615 (4.4);6.2659 (0.6); 6.2495 (0.6); 4.8504 (1.1); 4.8456 (1.1); 4.8194 (1.9);4.8146 (1.8); 4.7644 (1.3); 4.7552 (1.4); 4.7474 (1.4); 4.7382 (1.4);4.7332 (2.0); 4.7283 (1.9); 4.7022 (1.1); 4.6973 (1.1); 2.5805 (0.5);2.5592 (16.0); 2.5139 (1.6); 2.5090 (2.9); 2.5042 (1.4); 2.3363 (0.6);2.3270 (0.6); 2.3225 (0.8); 2.3133 (0.8); 2.3088 (0.6); 2.2995 (0.5);1.5613 (3.2); 1.0303 (6.9); 1.0166 (6.6); 0.9933 (6.8); 0.9796 (6.5);0.0061 (0.4); −0.0002 (5.9) I.14: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.2990(2.7); 6.3761 (0.5); 6.3487 (0.6); 4.7741 (1.2); 4.7593 (1.2); 4.7461(1.2); 4.7313 (1.2); 4.0464 (0.3); 4.0242 (0.4); 4.0111 (2.2); 3.9996(2.3); 3.9889 (2.3); 3.9779 (2.3); 3.9644 (0.4); 3.9426 (0.4); 2.5955(16.0); 2.3537 (0.4); 2.3388 (0.5); 2.3307 (0.6); 2.3158 (0.6); 2.3078(0.5); 2.2929 (0.5); 2.0557 (0.4); 2.0334 (0.8); 2.0111 (1.1); 1.9888(0.9); 1.9665 (0.5); 1.6273 (0.4); 1.0542 (6.5); 1.0313 (6.3); 1.0153(7.2); 1.0063 (13.8); 0.9923 (7.1); 0.9839 (13.1); 0.0350 (3.2) I.15:¹H-NMR(300.2 MHz, CDCl3): δ = 7.2991 (6.3); 6.1941 (0.5); 6.1676 (0.5);4.9561 (1.9); 4.9041 (3.7); 4.8023 (1.6); 4.7985 (4.0); 4.7863 (1.3);4.7747 (1.2); 4.7583 (1.2); 4.7465 (2.0); 2.5955 (16.0); 2.3810 (0.5);2.3644 (0.5); 2.3581 (0.6); 2.3417 (0.6); 2.3353 (0.5); 2.3187 (0.5);1.5948 (3.9); 1.1005 (6.3); 1.0776 (6.1); 1.0599 (6.4); 1.0369 (6.2);0.0370 (8.1) I.16: ¹H-NMR(499.9 MHz, CDCl3): δ = 7.2637 (2.6); 6.2129(0.6); 6.1966 (0.7); 5.5218 (0.8); 5.5198 (0.8); 5.5092 (1.4); 5.4987(0.8); 5.4966 (0.8); 5.4860 (0.3); 4.9335 (0.9); 4.9220 (1.8); 4.9203(1.8); 4.9087 (1.8); 4.9072 (1.9); 4.8955 (0.9); 4.8944 (0.9); 4.7470(1.3); 4.7378 (1.4); 4.7302 (1.3); 4.7210 (1.2); 4.7023 (1.0); 4.7010(1.0); 4.6918 (1.0); 4.6904 (1.1); 4.6868 (1.0); 4.6856 (1.0); 4.6763(0.8); 4.6751 (0.8); 4.6535 (1.0); 4.6525 (0.9); 4.6430 (1.0); 4.6418(1.0); 4.6381 (1.0); 4.6368 (0.9); 4.6276 (0.8); 4.6264 (0.8); 2.5771(0.4); 2.5532 (16.0); 2.3467 (0.5); 2.3373 (0.6); 2.3329 (0.7); 2.3236(0.7); 2.3192 (0.6); 2.3099 (0.5); 1.1183 (0.4); 1.1051 (0.3); 1.0472(6.5); 1.0335 (6.3); 1.0025 (6.6); 0.9887 (6.4); −0.0002 (2.6) I.17:¹H-NMR(300.2 MHz, CDCl3): δ = 7.2987 (1.9); 6.2581 (0.6); 6.2303 (0.6);5.7442 (0.9); 5.7176 (1.5); 5.6914 (1.0); 4.7086 (1.2); 4.6935 (1.3);4.6806 (1.2); 4.6654 (1.2); 3.6013 (0.9); 3.5733 (1.3); 3.5692 (1.2);3.5538 (0.8); 3.5412 (1.1); 3.5216 (1.6); 3.4940 (1.2); 3.3963 (0.4);3.3906 (0.9); 3.3852 (1.1); 3.3760 (0.9); 3.3706 (0.6); 3.3662 (1.3);3.3591 (1.7); 3.3512 (1.3); 3.3420 (0.8); 3.3329 (0.8); 3.3298 (0.6);3.3268 (0.6); 3.3213 (0.4); 2.6073 (0.4); 2.5850 (16.0); 2.3404 (0.5);2.3250 (0.5); 2.3175 (0.7); 2.3022 (0.6); 2.2946 (0.5); 2.2793 (0.5);1.0560 (6.4); 1.0331 (6.3); 1.0120 (6.6); 0.9890 (6.3); 0.0323 (2.0)I.18: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.2990 (5.6); 6.1603 (0.7); 6.1337(0.7); 5.3964 (0.6); 5.3828 (0.8); 5.3705 (1.2); 5.3579 (0.8); 5.3445(0.7); 5.3379 (0.7); 5.3329 (0.4); 4.7278 (1.2); 4.7115 (1.3); 4.7008(1.2); 4.6845 (1.2); 4.6621 (1.3); 4.6520 (0.5); 4.6363 (1.3); 4.6257(0.5); 4.6204 (0.7); 4.6100 (1.8); 4.5946 (0.6); 4.5841 (1.7); 4.3368(0.6); 4.3244 (1.1); 4.3163 (0.6); 4.3125 (0.6); 4.3056 (0.4); 4.2846(0.4); 4.2782 (0.4); 4.2720 (0.6); 4.2665 (0.4); 4.2594 (0.4); 4.2350(0.5); 4.2278 (0.5); 4.2223 (0.9); 4.2096 (0.6); 4.1818 (0.5); 4.1771(0.4); 4.1695 (0.8); 4.1576 (0.4); 2.6387 (0.3); 2.5896 (16.0); 2.3726(0.5); 2.3563 (0.5); 2.3502 (0.7); 2.3336 (0.7); 2.3275 (0.6); 2.3107(0.5); 1.6050 (3.6); 1.0994 (6.4); 1.0765 (6.2); 1.0514 (6.6); 1.0284(6.4); 0.0360 (5.9) I.19: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.2984 (4.7);6.3045 (0.7); 6.2825 (0.7); 5.4320 (0.8); 5.4246 (0.8); 5.4169 (1.2);5.4116 (1.2); 5.4052 (0.8); 5.3966 (0.8); 4.7447 (1.2); 4.7298 (1.3);4.7168 (1.2); 4.7019 (1.2); 3.9980 (1.1); 3.9833 (1.2); 3.9624 (3.6);3.9472 (2.9); 3.9364 (1.9); 3.9166 (2.2); 3.9020 (1.0); 3.8785 (1.5);3.8410 (0.6); 2.6112 (1.0); 2.5932 (16.0); 2.3510 (0.4); 2.3283 (0.7);2.3227 (0.6); 2.3128 (0.6); 2.3070 (0.8); 2.2912 (0.8); 2.2847 (0.6);2.2738 (0.8); 2.2633 (0.4); 2.2546 (0.6); 2.2457 (0.7); 2.2363 (0.4);2.2282 (0.8); 2.2176 (0.4); 2.2082 (0.5); 2.2003 (0.4); 2.1286 (0.5);2.1059 (0.3); 2.0819 (0.5); 2.0660 (0.6); 2.0421 (0.3); 1.1396 (0.5);1.1356 (0.5); 1.1176 (0.6); 1.0578 (7.3); 1.0349 (7.1); 1.0149 (7.3);0.9919 (7.0); 0.0343 (5.8) I.20: ¹H-NMR(499.9 MHz, CDCl3): δ = 7.1612(2.7); 6.2456 (0.7); 6.2292 (0.7); 4.6155 (1.2); 4.6065 (1.3); 4.5987(1.2); 4.5897 (1.2); 3.8048 (1.3); 3.7765 (3.7); 3.7478 (3.7); 3.7196(1.3); 2.4560 (16.0); 2.1647 (0.5); 2.1556 (0.6); 2.1510 (0.7); 2.1419(0.7); 2.1373 (0.6); 2.1281 (0.5); 1.4819 (1.1); 0.8965 (6.7); 0.8828(6.5); 0.8665 (6.8); 0.8527 (6.5); 0.0062 (3.1); −0.0002 (47.4); −0.0068(2.2); −0.1019 (3.3) I.21: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.6718 (0.9);8.6545 (0.9); 8.3154 (0.7); 4.4049 (0.9); 4.3869 (1.4); 4.3689 (1.0);4.1414 (0.6); 4.1346 (0.7); 4.1236 (2.1); 4.1170 (2.1); 4.1058 (2.2);4.0993 (2.1); 4.0881 (0.8); 4.0816 (0.6); 3.3277 (9.2); 2.5207 (0.5);2.5121 (5.4); 2.5077 (10.9); 2.5031 (14.3); 2.4985 (10.4); 2.4940 (5.1);2.4192 (16.0); 1.3773 (6.7); 1.3590 (6.6); 1.2384 (0.6); 1.2116 (4.7);1.1939 (9.7); 1.1761 (4.5); −0.0002 (2.1) I.22: ¹H-NMR(400.2 MHz,d₆-DMSO): δ = 8.5812 (1.1); 8.5623 (1.1); 8.3154 (1.4); 4.2932 (1.0);4.2750 (1.8); 4.2569 (1.0); 3.6617 (16.0); 3.3265 (9.6); 3.3025 (0.6);2.5069 (12.7); 2.5026 (16.6); 2.4982 (12.5); 2.3981 (15.4); 1.9313(0.5); 1.9270 (0.4); 1.9208 (0.5); 1.9152 (0.6); 1.9098 (0.6); 1.8990(0.5); 1.8927 (0.4); 1.4939 (0.3); 1.4831 (0.4); 1.4756 (0.4); 1.4602(0.6); 1.4493 (0.5); 1.4415 (0.5); 1.4307 (0.5); 1.2860 (0.5); 1.2674(0.7); 1.2461 (0.7); 1.2339 (0.7); 1.2119 (0.4); 0.8990 (6.5); 0.8817(7.1); 0.8596 (6.7); 0.8409 (2.8); −0.0002 (1.9) I.23: ¹H-NMR(400.2 MHz,d₆-DMSO): δ = 9.2313 (3.1); 8.6161 (1.3); 8.5969 (1.3); 8.3148 (0.4);7.0655 (3.6); 7.0444 (4.0); 6.6837 (0.5); 6.6767 (4.5); 6.6556 (4.1);6.6487 (0.4); 4.4879 (0.4); 4.4746 (0.5); 4.4688 (0.6); 4.4629 (0.7);4.4555 (0.6); 4.4497 (0.6); 4.4437 (0.6); 4.4304 (0.4); 4.1286 (0.8);4.1257 (0.9); 4.1109 (2.6); 4.1081 (2.7); 4.0930 (2.8); 4.0905 (2.6);4.0750 (1.0); 3.3321 (12.1); 3.0456 (0.6); 3.0325 (0.7); 3.0110 (1.1);2.9980 (1.0); 2.9317 (1.1); 2.9063 (1.1); 2.8972 (0.7); 2.8717 (0.7);2.5252 (0.4); 2.5203 (0.6); 2.5117 (8.5); 2.5073 (17.0); 2.5028 (22.1);2.4982 (16.0); 2.4937 (7.7); 2.2707 (16.0); 1.2386 (0.5); 1.1761 (5.0);1.1583 (10.4); 1.1406 (4.8); −0.0002 (3.3) I.24: ¹H-NMR(400.2 MHz,d₆-DMSO): δ = 8.6736 (0.8); 8.6549 (0.8); 8.3120 (1.2); 4.4937 (0.6);4.4788 (0.6); 4.1601 (0.4); 4.1506 (0.6); 4.1423 (1.5); 4.1326 (1.6);4.1245 (1.6); 4.1149 (1.5); 4.1064 (0.7); 4.0972 (0.4); 3.3267 (13.5);3.3028 (0.4); 2.5808 (0.7); 2.5639 (0.9); 2.5578 (0.7); 2.5463 (0.7);2.5378 (1.2); 2.5124 (6.7); 2.5079 (13.4); 2.5033 (17.5); 2.4987 (12.5);2.4942 (6.1); 2.3832 (13.1); 2.0569 (16.0); 2.0468 (1.3); 2.0318 (0.8);2.0268 (0.9); 2.0218 (0.5); 2.0130 (0.3); 2.0062 (0.4); 1.2188 (3.6);1.2010 (7.6); 1.1833 (3.4); −0.0002 (1.6) I.25: ¹H-NMR(400.2 MHz,d₆-DMSO): δ = 8.5474 (0.8); 8.5281 (0.8); 8.3108 (0.3); 4.2166 (1.2);4.1979 (1.6); 4.1898 (0.8); 4.1803 (1.6); 4.1721 (0.7); 4.1627 (1.6);4.1451 (2.0); 4.1277 (2.0); 4.1101 (1.6); 4.1008 (0.7); 4.0924 (0.5);4.0831 (0.7); 3.3279 (24.7); 2.5256 (0.4); 2.5209 (0.7); 2.5123 (8.8);2.5079 (17.6); 2.5033 (23.1); 2.4987 (16.8); 2.4942 (8.2); 2.3701(16.0); 2.1824 (0.6); 2.1653 (1.0); 2.1483 (1.0); 2.1312 (0.6); 1.2397(0.5); 1.2244 (4.4); 1.2067 (9.0); 1.1889 (4.3); 0.9701 (6.1); 0.9520(8.5); 0.9337 (5.7); −0.0002 (1.7) I.26: ¹H-NMR(400.2 MHz, d₆-DMSO): δ =8.6908 (0.9); 8.6716 (1.0); 8.3114 (3.3); 7.3143 (0.4); 7.3005 (0.7);7.2952 (2.7); 7.2865 (3.3); 7.2799 (10.4); 7.2695 (0.6); 7.2654 (0.8);7.2379 (0.7); 7.2323 (0.8); 7.2226 (0.8); 7.2164 (0.9); 7.2080 (0.4);7.2015 (0.4); 4.5934 (0.4); 4.5803 (0.5); 4.5741 (0.5); 4.5679 (0.6);4.5610 (0.5); 4.5549 (0.5); 4.5486 (0.5); 4.5354 (0.4); 4.1404 (1.0);4.1228 (3.3); 4.1052 (3.5); 4.0875 (1.2); 3.3323 (29.2); 3.3081 (1.3);3.1845 (0.7); 3.1713 (0.7); 3.1501 (1.2); 3.1369 (1.0); 3.0625 (1.2);3.0367 (1.2); 3.0282 (0.8); 3.0024 (0.7); 2.5259 (0.5); 2.5212 (0.8);2.5126 (9.6); 2.5081 (19.2); 2.5035 (25.0); 2.4989 (18.0); 2.4944 (8.7);2.2049 (16.0); 1.2393 (0.4); 1.1781 (4.6); 1.1604 (9.8); 1.1426 (4.5);−0.0002 (1.9) I.27: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.6725 (0.7); 8.6556(0.7); 8.3103 (3.2); 4.4126 (0.8); 4.3946 (1.2); 4.3766 (0.8); 4.1439(0.6); 4.1374 (0.7); 4.1261 (2.0); 4.1198 (2.0); 4.1083 (2.0); 4.1021(2.0); 4.0906 (0.7); 4.0844 (0.6); 3.3335 (26.6); 3.3092 (1.4); 2.5262(0.4); 2.5213 (0.6); 2.5128 (8.0); 2.5084 (15.6); 2.5038 (20.0); 2.4993(14.3); 2.4948 (6.9); 2.3830 (16.0); 1.3841 (6.6); 1.3658 (6.6); 1.2396(0.3); 1.2146 (4.4); 1.1968 (9.0); 1.1791 (4.3); −0.0002 (1.2) I.28:¹H-NMR(400.1 MHz, CDCl3): δ = 7.2614 (9.2); 6.3149 (1.0); 4.0958 (5.6);4.0843 (5.5); 2.5044 (16.0); 1.5556 (11.5); 1.5030 (47.7); −0.0002 (4.5)I.29: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.5780 (0.8); 8.5588 (0.8); 8.3113(0.6); 4.2438 (1.1); 4.2254 (1.7); 4.2071 (1.1); 3.6688 (16.0); 3.3268(16.9); 2.5256 (0.4); 2.5208 (0.6); 2.5121 (8.0); 2.5077 (15.9); 2.5032(20.6); 2.4986 (14.8); 2.4941 (7.2); 2.3703 (15.7); 2.1803 (0.5); 2.1632(0.9); 2.1461 (1.0); 2.1291 (0.6); 1.2396 (0.4); 0.9656 (6.1); 0.9487(6.1); 0.9403 (6.0); 0.9232 (5.6); −0.0002 (1.7) I.30: ¹H-NMR(400.2 MHz,d₆-DMSO): δ = 8.6808 (0.6); 8.6624 (0.7); 8.3101 (2.2); 4.5280 (0.5);4.5140 (0.5); 3.6707 (12.6); 3.3296 (16.6); 3.3054 (0.9); 2.5788 (0.7);2.5627 (0.8); 2.5605 (0.8); 2.5507 (0.6); 2.5448 (0.7); 2.5311 (1.2);2.5264 (0.5); 2.5127 (7.3); 2.5083 (13.5); 2.5037 (17.2); 2.4991 (12.5);2.4947 (6.0); 2.3847 (13.0); 2.0697 (0.6); 2.0662 (0.5); 2.0549 (16.0);2.0466 (0.9); 2.0367 (0.8); 2.0303 (0.8); 2.0246 (0.5); 2.0178 (0.3);2.0094 (0.4); −0.0002 (1.3) I.31: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.6854(0.5); 8.6711 (1.0); 8.6571 (0.5); 3.9968 (4.2); 3.9822 (4.2); 3.6650(15.9); 3.3779 (94.9); 2.5282 (0.4); 2.5234 (0.5); 2.5148 (6.6); 2.5105(13.2); 2.5060 (17.3); 2.5016 (12.8); 2.4973 (6.5); 2.4053 (16.0);−0.0002 (0.5) I.32: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.5931 (0.9); 8.5741(0.9); 4.2961 (1.1); 4.2779 (1.9); 4.2596 (1.1); 3.6636 (16.0); 3.3571(87.2); 2.5264 (0.4); 2.5217 (0.8); 2.5130 (9.0); 2.5087 (17.6); 2.5042(22.6); 2.4996 (16.2); 2.4951 (7.8); 2.3625 (15.7); 1.9388 (0.4); 1.9341(0.4); 1.9281 (0.4); 1.9226 (0.4); 1.9168 (0.5); 1.9108 (0.4); 1.9062(0.4); 1.4875 (0.3); 1.4797 (0.4); 1.4689 (0.4); 1.4644 (0.5); 1.4537(0.5); 1.4457 (0.5); 1.4350 (0.4); 1.2889 (0.5); 1.2704 (0.7); 1.2542(0.6); 1.2486 (0.8); 1.2367 (1.1); 1.2147 (0.4); 0.9019 (6.1); 0.8847(6.3); 0.8805 (3.8); 0.8617 (6.3); 0.8431 (2.6) I.33: ¹H-NMR(400.2 MHz,d₆-DMSO): δ = 8.6403 (1.0); 8.6209 (1.0); 4.4022 (0.4); 4.3909 (0.6);4.3830 (0.5); 4.3768 (0.6); 4.3718 (0.7); 4.3647 (0.6); 4.3578 (0.5);4.3454 (0.5); 4.1580 (0.4); 4.1488 (0.6); 4.1400 (0.5); 4.1370 (0.7);4.1310 (1.8); 4.1193 (1.9); 4.1132 (1.9); 4.1016 (1.8); 4.0954 (0.7);4.0927 (0.5); 4.0839 (0.6); 4.0746 (0.4); 3.3276 (22.3); 2.5256 (0.5);2.5120 (9.8); 2.5079 (18.5); 2.5034 (23.5); 2.4989 (16.9); 2.4945 (8.1);2.3741 (16.0); 1.7675 (0.3); 1.7556 (0.5); 1.7409 (0.4); 1.7350 (0.5);1.7289 (0.6); 1.7237 (0.7); 1.6986 (0.8); 1.6871 (0.5); 1.6708 (0.5);1.6666 (0.5); 1.6540 (0.5); 1.5904 (0.7); 1.5780 (0.5); 1.5687 (0.5);1.5575 (0.9); 1.5464 (0.5); 1.5365 (0.4); 1.2396 (0.5); 1.2126 (4.5);1.1949 (9.2); 1.1771 (4.3); 0.9290 (5.8); 0.9130 (5.5); 0.8934 (5.6);0.8774 (5.5); −0.0002 (1.6) I.34: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.6967(0.7); 8.3111 (5.2); 7.3868 (4.2); 7.3838 (2.7); 7.3755 (11.1); 7.3660(1.0); 7.3570 (1.2); 7.3488 (1.0); 7.3437 (0.6); 7.3355 (0.8); 5.1644(8.1); 4.0530 (1.8); 4.0439 (1.9); 3.3322 (22.9); 3.3081 (1.6); 2.5258(0.4); 2.5210 (0.7); 2.5125 (7.8); 2.5080 (15.4); 2.5034 (19.9); 2.4987(14.3); 2.4942 (6.8); 2.3883 (16.0); −0.0002 (1.6) I.35: ¹H-NMR(400.2MHz, d₆-DMSO): δ = 8.6811 (0.8); 8.6624 (0.8); 8.3098 (1.3); 4.5482(0.3); 4.5332 (0.4); 4.5281 (0.6); 4.5136 (0.6); 4.5087 (0.5); 4.4937(0.3); 3.6706 (12.7); 3.3308 (24.4); 3.3071 (0.6); 2.5787 (0.7); 2.5626(0.8); 2.5606 (0.8); 2.5507 (0.7); 2.5448 (0.8); 2.5311 (1.3); 2.5266(0.6); 2.5127 (7.6); 2.5083 (14.0); 2.5038 (18.0); 2.4992 (13.3); 2.4949(6.5); 2.3847 (13.1); 2.0694 (0.6); 2.0663 (0.6); 2.0549 (16.0); 2.0366(0.9); 2.0302 (0.9); 2.0245 (0.5); 2.0179 (0.4); 2.0093 (0.4); −0.0002(1.1) I.36: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.6905 (0.7); 8.6725 (0.7);4.5269 (0.5); 4.5119 (0.5); 3.6693 (12.7); 3.3460 (49.0); 2.5791 (0.7);2.5629 (0.8); 2.5608 (0.8); 2.5511 (0.6); 2.5448 (0.7); 2.5315 (1.2);2.5260 (0.5); 2.5124 (7.7); 2.5080 (14.1); 2.5034 (18.2); 2.4988 (13.4);2.4944 (6.4); 2.3833 (13.0); 2.0680 (0.6); 2.0646 (0.6); 2.0542 (16.0);2.0448 (0.9); 2.0351 (0.8); 2.0285 (0.8); 2.0229 (0.5); 2.0163 (0.4);2.0078 (0.4); 1.2386 (0.4); −0.0002 (0.4) I.37: ¹H-NMR(400.2 MHz,d₆-DMSO): δ = 8.6536 (0.9); 8.6345 (1.0); 4.4017 (0.4); 4.3903 (0.5);4.3824 (0.4); 4.3761 (0.5); 4.3711 (0.6); 4.3639 (0.5); 4.3570 (0.4);4.3448 (0.5); 4.1578 (0.4); 4.1486 (0.5); 4.1399 (0.5); 4.1369 (0.7);4.1308 (1.8); 4.1192 (1.9); 4.1130 (1.9); 4.1015 (1.8); 4.0952 (0.7);4.0924 (0.5); 4.0838 (0.6); 4.0745 (0.4); 3.3596 (80.0); 2.5271 (0.4);2.5223 (0.6); 2.5137 (8.1); 2.5092 (16.2); 2.5046 (21.0); 2.5000 (15.2);2.4955 (7.4); 2.3732 (16.0); 1.7672 (0.3); 1.7554 (0.4); 1.7408 (0.4);1.7349 (0.4); 1.7288 (0.6); 1.7234 (0.7); 1.6978 (0.8); 1.6850 (0.4);1.6808 (0.4); 1.6686 (0.4); 1.6641 (0.4); 1.6518 (0.4); 1.6480 (0.4);1.5908 (0.7); 1.5784 (0.5); 1.5689 (0.4); 1.5580 (0.8); 1.5468 (0.5);1.5368 (0.4); 1.2391 (0.5); 1.2101 (4.5); 1.1923 (9.3); 1.1746 (4.3);0.9281 (5.5); 0.9121 (5.2); 0.8920 (5.2); 0.8760 (5.2) I.38:¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.6900 (1.0); 8.6708 (1.0); 8.3115(1.5); 7.3142 (0.4); 7.2950 (2.7); 7.2864 (3.3); 7.2799 (10.4); 7.2693(0.6); 7.2654 (0.8); 7.2378 (0.7); 7.2321 (0.8); 7.2226 (0.8); 7.2162(0.9); 7.2080 (0.4); 7.2014 (0.4); 4.5933 (0.4); 4.5803 (0.5); 4.5740(0.5); 4.5678 (0.7); 4.5608 (0.6); 4.5547 (0.6); 4.5484 (0.6); 4.5352(0.4); 4.1405 (1.0); 4.1229 (3.3); 4.1053 (3.5); 4.0875 (1.2); 3.3295(22.9); 3.3055 (0.6); 3.1844 (0.7); 3.1712 (0.7); 3.1499 (1.2); 3.1369(1.0); 3.0624 (1.2); 3.0367 (1.2); 3.0281 (0.8); 3.0024 (0.7); 2.5257(0.5); 2.5209 (0.8); 2.5123 (10.1); 2.5079 (19.9); 2.5034 (25.7); 2.4988(18.5); 2.4943 (8.9); 2.2050 (16.0); 1.2397 (0.4); 1.1782 (4.6); 1.1605(9.6); 1.1427 (4.4); −0.0002 (1.9) I.39: ¹H-NMR(400.2 MHz, d₆-DMSO): δ =9.2514 (2.6); 8.6265 (1.2); 8.6072 (1.3); 7.0685 (3.3); 7.0473 (3.6);6.6844 (0.5); 6.6774 (4.2); 6.6727 (1.3); 6.6610 (1.2); 6.6562 (3.9);6.6491 (0.4); 4.4934 (0.4); 4.4802 (0.5); 4.4742 (0.5); 4.4684 (0.6);4.4610 (0.6); 4.4551 (0.5); 4.4491 (0.6); 4.4358 (0.4); 4.1303 (0.7);4.1273 (0.8); 4.1125 (2.3); 4.1096 (2.4); 4.0947 (2.5); 4.0920 (2.3);4.0767 (0.9); 3.3686 (95.7); 3.3653 (83.9); 3.3630 (90.8); 3.0518 (0.6);3.0386 (0.6); 3.0172 (1.0); 3.0041 (0.9); 2.9377 (1.0); 2.9124 (1.0);2.9032 (0.7); 2.8779 (0.6); 2.5268 (0.7); 2.5219 (1.1); 2.5135 (14.1);2.5090 (28.2); 2.5044 (36.7); 2.4998 (26.4); 2.4953 (12.7); 2.2313(16.0); 1.2389 (0.6); 1.1761 (4.7); 1.1584 (10.0); 1.1406 (4.5); −0.0002(2.0) I.40: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.5609 (0.8); 8.5416 (0.8);4.2142 (1.2); 4.1967 (1.6); 4.1954 (1.6); 4.1894 (0.8); 4.1779 (1.3);4.1716 (0.7); 4.1623 (1.6); 4.1446 (2.0); 4.1272 (2.1); 4.1095 (1.6);4.1002 (0.7); 4.0918 (0.5); 4.0824 (0.7); 3.3649 (92.0); 2.5272 (0.4);2.5222 (0.7); 2.5138 (8.6); 2.5093 (17.2); 2.5047 (22.3); 2.5001 (16.0);2.4956 (7.6); 2.3690 (16.0); 2.1804 (0.5); 2.1634 (0.9); 2.1463 (0.9);2.1293 (0.6); 1.2387 (0.6); 1.2217 (4.5); 1.2040 (9.3); 1.1862 (4.4);0.9695 (5.9); 0.9522 (7.3); 0.9500 (7.0); 0.9326 (5.5) I.41:¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.6430 (0.4); 8.6288 (0.8); 8.6146(0.4); 8.3108 (1.2); 4.9724 (0.4); 4.9567 (1.1); 4.9411 (1.5); 4.9255(1.1); 4.9099 (0.4); 3.9385 (3.3); 3.9240 (3.3); 3.3286 (18.1); 3.3045(0.5); 2.5261 (0.4); 2.5212 (0.6); 2.5126 (7.2); 2.5082 (14.4); 2.5037(18.6); 2.4991 (13.4); 2.4947 (6.5); 2.4037 (16.0); 1.2153 (15.9);1.1996 (15.7); −0.0002 (1.4) I.42: ¹H-NMR(400.2 MHz, d₆-DMSO): δ =8.6724 (0.8); 8.6551 (0.8); 8.3108 (0.7); 4.4126 (1.0); 4.3946 (1.6);4.3766 (1.0); 4.1439 (0.6); 4.1374 (0.7); 4.1261 (2.0); 4.1198 (2.0);4.1083 (2.0); 4.1021 (2.0); 4.0905 (0.7); 4.0844 (0.6); 3.3317 (29.5);3.3081 (0.3); 2.5260 (0.4); 2.5127 (7.7); 2.5083 (15.0); 2.5037 (19.4);2.4991 (14.0); 2.4947 (6.8); 2.3830 (16.0); 1.3839 (6.5); 1.3657 (6.4);1.2144 (4.3); 1.1967 (8.9); 1.1789 (4.2); −0.0002 (1.3) I.43:¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.9195 (2.0); 4.0933 (1.3); 4.0756(4.2); 4.0579 (4.2); 4.0401 (1.3); 3.3493 (68.1); 2.5263 (0.4); 2.5215(0.6); 2.5128 (7.5); 2.5084 (15.0); 2.5038 (19.5); 2.4992 (14.1); 2.4947(6.8); 2.3689 (16.0); 1.4425 (1.1); 1.4304 (2.9); 1.4221 (3.1); 1.4112(1.3); 1.2388 (0.3); 1.1749 (1.5); 1.1689 (4.9); 1.1641 (3.3); 1.1556(3.4); 1.1513 (9.6); 1.1436 (1.3); 1.1335 (4.3); −0.0002 (1.1) I.44:¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.5590 (0.9); 8.5399 (0.9); 4.2145(1.2); 4.1967 (1.8); 4.1894 (0.8); 4.1783 (1.4); 4.1715 (0.7); 4.1622(1.6); 4.1446 (2.0); 4.1271 (2.0); 4.1095 (1.6); 4.1002 (0.7); 4.0918(0.5); 4.0824 (0.7); 3.3452 (65.9); 2.5258 (0.5); 2.5124 (9.5); 2.5080(18.5); 2.5034 (23.6); 2.4988 (16.9); 2.4944 (8.1); 2.3691 (16.0);2.1803 (0.6); 2.1633 (1.0); 2.1462 (1.0); 2.1292 (0.6); 1.2390 (0.5);1.2216 (4.5); 1.2038 (9.1); 1.1861 (4.3); 0.9695 (6.3); 0.9521 (8.1);0.9326 (5.8); −0.0002 (1.2) I.45: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.7008(1.4); 8.6815 (1.4); 7.3164 (0.6); 7.2970 (3.2); 7.2872 (4.4); 7.2816(11.0); 7.2667 (1.0); 7.2400 (0.8); 7.2346 (1.0); 7.2253 (1.0); 7.2186(1.1); 7.2102 (0.6); 7.2034 (0.5); 4.5939 (0.5); 4.5806 (0.7); 4.5746(0.7); 4.5684 (0.8); 4.5614 (0.7); 4.5551 (0.7); 4.5490 (0.7); 4.5358(0.5); 4.1390 (1.2); 4.1214 (3.7); 4.1037 (3.8); 4.0860 (1.3); 3.3510(98.3); 3.1844 (0.8); 3.1713 (0.8); 3.1501 (1.3); 3.1371 (1.2); 3.0614(1.3); 3.0356 (1.3); 3.0271 (0.9); 3.0013 (0.8); 2.5081 (23.1); 2.5037(28.5); 2.4993 (20.7); 2.2039 (16.0); 1.2383 (0.7); 1.1746 (4.7); 1.1568(9.5); 1.1391 (4.5); −0.0002 (0.7) I.46: ¹H-NMR(400.2 MHz, d₆-DMSO): δ =8.5881 (0.8); 8.5689 (0.8); 4.2420 (1.1); 4.2241 (1.6); 4.2053 (1.1);3.6681 (16.0); 3.3468 (61.3); 2.5260 (0.4); 2.5213 (0.5); 2.5126 (7.2);2.5081 (14.4); 2.5035 (18.7); 2.4989 (13.4); 2.4944 (6.4); 2.3693(15.6); 2.1785 (0.5); 2.1613 (0.9); 2.1443 (0.9); 2.1272 (0.6); 1.2390(0.4); 0.9649 (5.8); 0.9479 (5.8); 0.9390 (5.6); 0.9220 (5.3); −0.0002(0.9) I.47: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.6834 (0.8); 8.6646 (0.8);4.5130 (0.3); 4.4978 (0.4); 4.4931 (0.6); 4.4781 (0.6); 4.4738 (0.5);4.4584 (0.3); 4.1593 (0.4); 4.1497 (0.6); 4.1415 (1.5); 4.1317 (1.6);4.1237 (1.6); 4.1140 (1.5); 4.1056 (0.6); 4.0963 (0.4); 3.3489 (62.0);2.5813 (0.6); 2.5646 (0.8); 2.5580 (0.6); 2.5468 (0.6); 2.5381 (1.2);2.5258 (0.5); 2.5128 (7.1); 2.5083 (14.3); 2.5037 (18.8); 2.4990 (13.4);2.4945 (6.4); 2.3820 (13.0); 2.0563 (16.0); 2.0458 (1.2); 2.0420 (0.8);2.0308 (0.8); 2.0257 (0.9); 2.0205 (0.5); 2.0118 (0.3); 2.0050 (0.4);1.2388 (0.4); 1.2161 (3.6); 1.1984 (7.6); 1.1807 (3.4); −0.0002 (0.9)I.48: ¹H-NMR(499.9 MHz, d₆-DMSO): δ = 8.6674 (1.4); 8.6559 (2.3); 8.6444(1.1); 4.0600 (5.2); 4.0468 (10.0); 4.0337 (5.0); 3.9915 (8.4); 3.9798(8.1); 3.7102 (7.3); 3.3215 (9.0); 3.1463 (13.6); 2.5364 (0.4); 2.5114(2.7); 2.5079 (3.3); 2.5044 (2.4); 2.4418 (7.3); 2.4083 (30.6); 1.6384(0.9); 1.6239 (2.7); 1.6103 (5.0); 1.5957 (5.0); 1.5821 (2.5); 1.5677(0.6); 0.9091 (8.4); 0.8943 (16.0); 0.8794 (7.2) I.49: ¹H-NMR(300.2 MHz,CDCl3): δ = 7.4923 (0.3); 7.2989 (3.9); 6.3916 (0.5); 6.3644 (0.6);5.1699 (0.4); 5.1490 (1.0); 5.1282 (1.4); 5.1073 (1.0); 5.0864 (0.4);4.7153 (1.2); 4.7009 (1.3); 4.6875 (1.2); 4.6730 (1.2); 2.6476 (1.2);2.5976 (16.0); 2.4411 (0.9); 2.3587 (1.0); 2.3402 (0.5); 2.3256 (0.5);2.3172 (0.7); 2.3026 (0.7); 2.2943 (0.5); 2.2797 (0.5); 1.6249 (0.8);1.3363 (7.6); 1.3316 (8.1); 1.3153 (7.7); 1.3108 (8.1); 1.0442 (6.6);1.0213 (6.5); 1.0071 (6.8); 0.9841 (6.5); 0.0359 (4.1) I.50:¹H-NMR(300.2 MHz, d₆-DMSO): δ = 8.9269 (2.0); 3.6346 (16.0); 3.3469(6.1); 2.5345 (0.6); 2.5286 (1.2); 2.5225 (1.7); 2.5165 (1.2); 2.5106(0.6); 2.3931 (15.8); 1.4833 (1.0); 1.4668 (2.6); 1.4557 (3.0); 1.4414(1.3); 1.2147 (1.4); 1.2003 (2.9); 1.1892 (2.7); 1.1726 (1.0); 0.0193(1.2) I.51: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.7996 (2.3); 2.8919 (0.8);2.7333 (0.7); 2.7322 (0.7); 2.5210 (0.4); 2.5125 (4.1); 2.5081 (8.4);2.5035 (11.0); 2.4989 (7.9); 2.4944 (3.8); 2.3887 (1.7); 2.3706 (16.0);1.4114 (1.1); 1.3996 (2.7); 1.3914 (2.9); 1.3807 (1.3); 1.3753 (0.8);1.3568 (0.6); 1.1254 (1.3); 1.1147 (2.8); 1.1065 (2.8); 1.0946 (1.0);−0.0002 (7.8) I.52: ¹H-NMR(400.1 MHz, CDCl3): δ = 7.2604 (9.4); 6.3394(1.0); 6.3189 (1.0); 4.7313 (1.4); 4.7205 (1.4); 4.7103 (1.4); 4.6995(1.3); 4.0842 (1.0); 4.0656 (1.2); 4.0560 (1.9); 4.0374 (1.8); 3.9951(1.8); 3.9769 (1.8); 3.9669 (1.0); 3.9485 (0.9); 2.5620 (16.0); 2.5133(0.8); 2.3211 (0.6); 2.3042 (0.9); 2.2925 (0.9); 2.2754 (0.7); 1.5420(6.0); 1.1955 (0.4); 1.1832 (0.7); 1.1754 (0.7); 1.1640 (1.1); 1.1521(0.8); 1.1448 (1.1); 1.1272 (0.6); 1.0202 (7.9); 1.0029 (8.0); 0.9934(8.3); 0.9760 (7.7); 0.9527 (0.5); 0.6225 (0.8); 0.6097 (3.0); 0.5900(2.9); 0.5778 (0.8); 0.3245 (1.1); 0.3128 (3.3); 0.3008 (3.1); 0.2885(0.8); −0.0002 (9.8) 1.53: ¹H-NMR(400.1 MHz, CDCl3): δ = 7.2594 (9.0);6.3038 (0.9); 6.2837 (0.9); 5.0683 (1.1); 5.0498 (1.6); 5.0313 (1.1);4.6842 (1.3); 4.6733 (1.4); 4.6633 (1.3); 4.6524 (1.3); 2.5560 (16.0);2.3975 (1.2); 2.3796 (1.4); 2.3660 (1.3); 2.3489 (0.7); 2.3056 (0.7);2.2938 (0.7); 2.2887 (0.9); 2.2770 (0.9); 2.2718 (0.8); 2.2601 (0.6);2.1539 (0.7); 2.1338 (0.9); 2.1293 (0.9); 2.1108 (1.0); 2.0925 (0.9);2.0861 (0.9); 2.0614 (0.6); 1.8789 (0.4); 1.8527 (0.9); 1.8269 (0.9);1.8018 (0.3); 1.6862 (0.6); 1.6655 (1.0); 1.6396 (0.9); 1.6187 (0.4);1.5406 (7.5); 1.0083 (7.6); 0.9912 (7.7); 0.9728 (7.8); 0.9555 (7.3);−0.0002 (9.5) I.54: ¹H-NMR(400.1 MHz, CDCl3): δ = 7.3486 (0.6); 7.2595(9.4); 6.3215 (1.0); 6.3020 (1.0); 4.7145 (1.4); 4.7036 (1.4); 4.6942(1.4); 4.6833 (1.3); 4.2074 (0.3); 4.1913 (0.9); 4.1739 (0.9); 4.1635(1.2); 4.1475 (3.3); 4.1308 (3.3); 4.1149 (1.2); 4.1047 (0.6); 3.4468(0.3); 3.4310 (0.4); 2.5587 (16.0); 2.5143 (1.7); 2.3009 (0.7); 2.2843(1.0); 2.2724 (1.0); 2.2552 (0.7); 1.7407 (0.6); 1.7247 (1.7); 1.7073(3.2); 1.6898 (3.2); 1.6721 (1.7); 1.6535 (0.4); 1.5408 (6.9); 1.1159(0.9); 1.0986 (0.9); 1.0107 (8.1); 0.9933 (8.5); 0.9875 (6.5); 0.9749(9.2); 0.9687 (10.0); 0.9583 (8.6); 0.9492 (5.6); 0.9293 (1.8); 0.9107(0.5); −0.0002 (9.7); −0.0016 (9.7) I.55: ¹H-NMR(400.1 MHz, CDCl3): δ =7.2596 (8.2); 6.3204 (0.9); 6.3002 (0.9); 4.7089 (1.4); 4.6979 (1.4);4.6880 (1.3); 4.6769 (1.3); 4.2144 (0.6); 4.2044 (1.2); 4.1879 (3.2);4.1715 (3.2); 4.1554 (1.1); 4.1449 (0.5); 2.5843 (0.7); 2.5583 (16.0);2.2961 (0.6); 2.2792 (0.9); 2.2675 (0.9); 2.2504 (0.6); 1.6899 (0.5);1.6739 (1.6); 1.6532 (2.2); 1.6359 (2.0); 1.6192 (0.8); 1.5483 (2.3);1.4477 (0.4); 1.4294 (1.4); 1.4108 (2.4); 1.3918 (2.3); 1.3732 (1.3);1.3551 (0.3); 1.2491 (0.5); 1.2322 (0.5); 1.0085 (7.7); 0.9913 (7.6);0.9712 (8.4); 0.9662 (6.2); 0.9540 (8.3); 0.9471 (8.9); 0.9285 (3.7);−0.0002 (8.6) I.56: ¹H-NMR(400.1 MHz, CDCl3): δ = 7.2595 (8.6); 6.2836(1.1); 6.2640 (1.1); 4.6642 (1.4); 4.6531 (1.5); 4.6435 (1.4); 4.6322(1.4); 4.2198 (1.1); 4.2102 (1.4); 4.1985 (1.0); 4.1893 (0.4); 2.5737(0.6); 2.5578 (16.0); 2.2586 (0.7); 2.2413 (1.0); 2.2270 (1.0); 2.2122(0.7); 1.5416 (4.5); 1.0866 (0.4); 1.0705 (0.3); 0.9966 (7.9); 0.9795(7.7); 0.9540 (7.9); 0.9368 (7.6); 0.7910 (0.9); 0.7732 (3.7); 0.7574(6.2); 0.7336 (1.8); −0.0002 (9.0) I.57: ¹H-NMR(400.1 MHz, CDCl3): δ =7.3962 (0.5); 7.3643 (13.9); 7.3411 (0.8); 7.3280 (0.3); 7.2583 (9.0);6.2948 (1.0); 6.2743 (1.0); 5.2567 (1.6); 5.2264 (3.5); 5.1808 (3.5);5.1505 (1.5); 4.7627 (1.3); 4.7516 (1.4); 4.7417 (1.3); 4.7305 (1.3);2.5374 (16.0); 2.3031 (0.6); 2.2859 (0.9); 2.2743 (0.9); 2.2689 (0.8);2.2575 (0.6); 1.5387 (6.1); 0.9786 (7.4); 0.9614 (7.2); 0.9198 (7.5);0.9026 (7.2); −0.0002 (9.5) I.58: ¹H-NMR(400.1 MHz, CDCl3): δ = 7.2593(8.8); 6.2970 (1.0); 6.2770 (1.0); 5.9603 (0.6); 5.9466 (0.6); 5.9330(0.9); 5.9176 (1.0); 5.9037 (0.6); 5.8914 (0.7); 5.8768 (0.4); 5.3842(2.0); 5.3414 (1.7); 5.2997 (2.1); 5.2737 (1.9); 4.7448 (1.4); 4.7338(1.5); 4.7238 (1.8); 4.7126 (1.6); 4.6907 (1.9); 4.6732 (3.1); 4.6573(1.7); 4.6395 (0.4); 4.6249 (0.4); 2.5760 (0.7); 2.5570 (16.0); 2.3172(0.7); 2.3005 (1.0); 2.2862 (1.0); 2.2711 (0.7); 1.5410 (5.1); 1.1011(0.4); 1.0846 (0.5); 1.0155 (7.8); 0.9985 (7.7); 0.9767 (7.9); 0.9594(7.6); −0.0002 (9.0) I.59: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.2986 (11.6);6.2315 (0.4); 6.2038 (0.5); 4.8488 (1.2); 4.8334 (1.2); 4.8206 (1.2);4.8053 (1.3); 4.7793 (0.8); 4.7649 (0.4); 4.7516 (0.8); 4.7372 (1.0);4.7095 (1.0); 4.6818 (0.4); 4.5314 (0.3); 4.5037 (1.0); 4.4760 (1.1);4.4616 (0.8); 4.4483 (0.4); 4.4339 (0.8); 2.9948 (0.7); 2.9227 (0.6);2.9210 (0.6); 2.5940 (16.0); 2.3853 (0.4); 2.3698 (0.4); 2.3624 (0.6);2.3469 (0.6); 2.3396 (0.5); 2.3239 (0.4); 1.5881 (7.6); 1.0855 (6.1);1.0627 (5.9); 1.0411 (6.2); 1.0181 (6.0); 0.0484 (0.4); 0.0376 (12.4);0.0284 (0.4); 0.0267 (0.5) I.60: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.4710(1.0); 7.4693 (1.1); 7.4629 (0.5); 7.4448 (2.5); 7.4231 (0.9); 7.4177(2.0); 7.3292 (1.1); 7.3254 (0.6); 7.3102 (0.6); 7.3046 (1.6); 7.2981(4.8); 7.2833 (0.4); 7.2798 (0.5); 7.1597 (2.2); 7.1558 (2.9); 7.1487(0.7); 7.1309 (2.2); 7.1277 (1.8); 6.3872 (0.6); 6.3590 (0.6); 5.0168(1.2); 5.0017 (1.3); 4.9888 (1.2); 4.9736 (1.2); 2.6094 (16.0); 2.5512(0.4); 2.5359 (0.5); 2.5282 (0.6); 2.5130 (0.6); 2.5054 (0.5); 2.4901(0.5); 2.0430 (0.4); 1.5985 (1.6); 1.1772 (6.2); 1.1538 (10.8); 1.1296(6.0); 0.0381 (5.3) 1.61: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.2987 (0.6);4.6463 (0.5); 4.6324 (0.5); 4.6188 (0.5); 4.6049 (0.5); 2.5964 (6.0);1.5260 (16.0); 1.0332 (2.4); 1.0101 (2.5); 1.0044 (2.7); 0.9813 (2.3);0.0320 (0.7) I.62: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.5464 (1.0); 8.5272(1.0); 4.2137 (1.1); 4.2053 (0.3); 4.1950 (1.6); 4.1876 (0.8); 4.1777(1.6); 4.1698 (0.8); 4.1605 (1.7); 4.1428 (2.2); 4.1253 (2.2); 4.1076(1.7); 4.0983 (0.8); 4.0899 (0.5); 4.0806 (0.7); 3.3247 (9.9); 2.5119(4.5); 2.5074 (9.4); 2.5028 (12.4); 2.4982 (8.8); 2.4937 (4.2); 2.4047(16.0); 2.1760 (0.5); 2.1590 (1.0); 2.1420 (1.0); 2.1250 (0.6); 1.2215(4.8); 1.2038 (9.9); 1.1860 (4.6); 0.9661 (6.2); 0.9485 (9.7); 0.9305(5.7); −0.0002 (7.1) I.63: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.5741 (0.9);8.5548 (0.9); 4.2417 (1.0); 4.2235 (1.6); 4.2051 (1.1); 3.6668 (16.0);3.3250 (9.2); 2.5120 (3.8); 2.5075 (7.9); 2.5030 (10.4); 2.4983 (7.4);2.4938 (3.5); 2.4052 (15.2); 2.1743 (0.5); 2.1572 (0.9); 2.1401 (0.9);2.1231 (0.6); 0.9616 (5.9); 0.9446 (6.1); 0.9372 (5.8); 0.9202 (5.4);−0.0002 (6.8) I.64: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.5740 (0.9); 8.5547(0.9); 4.2421 (1.1); 4.2240 (1.6); 4.2055 (1.1); 3.6671 (16.0); 3.3246(6.8); 2.5121 (3.6); 2.5076 (7.4); 2.5030 (9.7); 2.4984 (6.9); 2.4939(3.2); 2.4054 (15.3); 2.1745 (0.5); 2.1574 (0.9); 2.1404 (1.0); 2.1233(0.6); 1.2382 (0.4); 0.9617 (6.1); 0.9448 (6.2); 0.9374 (6.0); 0.9203(5.5); −0.0002 (7.1) I.65: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.6889 (1.4);8.6696 (1.4); 7.3148 (0.6); 7.2956 (3.1); 7.2857 (4.2); 7.2801 (10.8);7.2688 (0.9); 7.2650 (1.1); 7.2381 (0.8); 7.2328 (1.0); 7.2236 (1.0);7.2167 (1.1); 7.2083 (0.6); 7.2016 (0.5); 4.5907 (0.5); 4.5775 (0.6);4.5713 (0.6); 4.5652 (0.8); 4.5583 (0.7); 4.5520 (0.7); 4.5458 (0.7);4.5326 (0.5); 4.1380 (1.2); 4.1205 (3.8); 4.1028 (3.9); 4.0850 (1.3);3.3278 (8.7); 3.1798 (0.7); 3.1668 (0.8); 3.1455 (1.3); 3.1324 (1.2);3.0573 (1.3); 3.0315 (1.3); 3.0230 (0.9); 2.9972 (0.8); 2.5117 (5.2);2.5075 (10.1); 2.5030 (12.9); 2.4985 (9.3); 2.4943 (4.5); 2.2451 (16.0);1.2380 (0.3); 1.1750 (4.9); 1.1573 (10.1); 1.1395 (4.7); −0.0002 (7.1)I.66: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.6890 (1.4); 8.6696 (1.4); 7.3172(0.4); 7.3148 (0.6); 7.3010 (0.9); 7.2959 (3.0); 7.2858 (3.9); 7.2800(10.6); 7.2688 (0.8); 7.2648 (1.0); 7.2382 (0.8); 7.2329 (0.9); 7.2238(0.9); 7.2167 (1.0); 7.2083 (0.6); 7.2015 (0.5); 4.5903 (0.5); 4.5771(0.6); 4.5709 (0.6); 4.5648 (0.7); 4.5579 (0.6); 4.5516 (0.6); 4.5454(0.6); 4.5322 (0.5); 4.1379 (1.1); 4.1204 (3.7); 4.1027 (3.9); 4.0849(1.3); 3.3277 (9.7); 3.1797 (0.7); 3.1665 (0.8); 3.1453 (1.2); 3.1322(1.1); 3.0570 (1.2); 3.0312 (1.2); 3.0227 (0.8); 2.9969 (0.7); 2.5205(0.4); 2.5120 (5.3); 2.5076 (10.5); 2.5030 (13.7); 2.4984 (9.7); 2.4939(4.6); 2.2451 (16.0); 1.2379 (0.3); 1.1750 (5.1); 1.1573 (10.6); 1.1395(4.9); −0.0002 (8.7) I.67: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.6895 (1.3);8.6701 (1.3); 7.3174 (0.4); 7.3148 (0.6); 7.3012 (0.8); 7.2961 (2.8);7.2945 (2.6); 7.2859 (3.6); 7.2801 (9.9); 7.2689 (0.7); 7.2647 (1.0);7.2383 (0.8); 7.2331 (0.9); 7.2240 (0.8); 7.2168 (1.0); 7.2083 (0.6);7.2016 (0.5); 4.5901 (0.4); 4.5769 (0.6); 4.5707 (0.6); 4.5645 (0.7);4.5576 (0.6); 4.5513 (0.6); 4.5451 (0.6); 4.5319 (0.5); 4.1375 (1.1);4.1200 (3.5); 4.1025 (3.8); 4.0847 (1.3); 3.3276 (10.1); 3.1794 (0.7);3.1662 (0.8); 3.1450 (1.2); 3.1319 (1.0); 3.0567 (1.2); 3.0309 (1.2);3.0224 (0.8); 2.9966 (0.7); 2.5206 (0.4); 2.5120 (5.0); 2.5075 (10.4);2.5029 (13.8); 2.4983 (9.8); 2.4937 (4.7); 2.2448 (16.0); 1.1746 (5.2);1.1569 (11.0); 1.1391 (5.0); 0.0080 (0.3); −0.0002 (9.7) I.68:¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.6356 (1.1); 8.6165 (1.1); 4.3980(0.3); 4.3867 (0.5); 4.3787 (0.4); 4.3725 (0.5); 4.3675 (0.6); 4.3604(0.5); 4.3535 (0.4); 4.3412 (0.4); 4.1565 (0.4); 4.1473 (0.6); 4.1387(0.5); 4.1352 (0.7); 4.1296 (1.9); 4.1175 (2.0); 4.1117 (2.0); 4.0998(1.9); 4.0939 (0.7); 4.0906 (0.5); 4.0821 (0.6); 4.0728 (0.4); 3.3259(11.2); 2.5125 (4.5); 2.5080 (9.2); 2.5035 (12.0); 2.4988 (8.5); 2.4943(4.0); 2.4106 (16.0); 2.2451 (0.4); 1.7486 (0.4); 1.7339 (0.4); 1.7281(0.4); 1.7220 (0.6); 1.7166 (0.7); 1.6962 (0.6); 1.6911 (0.6); 1.6845(0.5); 1.6683 (0.5); 1.6641 (0.5); 1.6517 (0.4); 1.6479 (0.4); 1.5861(0.6); 1.5736 (0.4); 1.5645 (0.5); 1.5534 (0.8); 1.5422 (0.5); 1.5325(0.3); 1.2381 (0.5); 1.2104 (4.6); 1.1926 (9.7); 1.1749 (4.5); 0.9266(5.5); 0.9106 (5.3); 0.8916 (5.2); 0.8756 (5.1); −0.0002 (6.0) I.69:¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.6361 (1.1); 8.6169 (1.1); 4.3976(0.4); 4.3864 (0.6); 4.3785 (0.5); 4.3723 (0.6); 4.3673 (0.7); 4.3601(0.6); 4.3533 (0.4); 4.3409 (0.5); 4.1564 (0.4); 4.1472 (0.6); 4.1385(0.5); 4.1350 (0.8); 4.1294 (1.9); 4.1174 (2.0); 4.1116 (2.0); 4.0997(1.9); 4.0938 (0.7); 4.0904 (0.5); 4.0820 (0.6); 4.0726 (0.4); 3.3262(12.2); 2.5124 (5.0); 2.5079 (10.0); 2.5034 (13.0); 2.4988 (9.2); 2.4943(4.3); 2.4104 (16.0); 1.7603 (0.3); 1.7484 (0.4); 1.7337 (0.4); 1.7279(0.4); 1.7217 (0.7); 1.7164 (0.7); 1.6910 (0.6); 1.6843 (0.6); 1.6681(0.5); 1.6638 (0.5); 1.6514 (0.4); 1.6477 (0.4); 1.5860 (0.6); 1.5735(0.4); 1.5643 (0.5); 1.5533 (0.9); 1.5420 (0.5); 1.5324 (0.4); 1.2384(0.4); 1.2101 (4.7); 1.1924 (9.7); 1.1746 (4.5); 0.9264 (5.7); 0.9105(5.4); 0.8915 (5.4); 0.8755 (5.3); −0.0002 (5.1) I.70: ¹H-NMR(400.2 MHz,d₆-DMSO): δ = 8.6774 (0.9); 8.6585 (0.9); 4.5419 (0.3); 4.5273 (0.4);4.5216 (0.6); 4.5075 (0.6); 4.5021 (0.5); 4.4873 (0.3); 3.6684 (12.4);3.3256 (8.1); 2.5763 (0.7); 2.5602 (0.8); 2.5580 (0.8); 2.5496 (0.6);2.5421 (0.6); 2.5299 (1.1); 2.5207 (0.4); 2.5120 (4.2); 2.5076 (7.7);2.5030 (9.9); 2.4984 (7.2); 2.4939 (3.4); 2.4207 (12.4); 2.0538 (16.0);2.0441 (1.2); 2.0390 (0.8); 2.0297 (0.8); 2.0229 (0.8); 2.0173 (0.5);2.0109 (0.3); 2.0021 (0.4); −0.0002 (6.5) I.71: ¹H-NMR(400.2 MHz,d₆-DMSO): δ = 8.6773 (0.8); 8.6585 (0.8); 4.5421 (0.3); 4.5275 (0.4);4.5218 (0.6); 4.5073 (0.6); 4.5023 (0.5); 4.4875 (0.3); 3.6686 (12.3);3.3254 (6.8); 2.5765 (0.7); 2.5604 (0.8); 2.5582 (0.8); 2.5499 (0.6);2.5423 (0.6); 2.5302 (1.1); 2.5207 (0.4); 2.5121 (3.8); 2.5077 (6.9);2.5031 (9.0); 2.4985 (6.6); 2.4940 (3.1); 2.4208 (12.4); 2.0540 (16.0);2.0444 (1.2); 2.0392 (0.8); 2.0299 (0.8); 2.0232 (0.8); 2.0175 (0.5);2.0111 (0.3); 2.0024 (0.4); −0.0002 (6.4) I.72: ¹H-NMR(400.2 MHz,d₆-DMSO): δ = 8.6773 (0.9); 8.6585 (0.9); 4.5422 (0.4); 4.5275 (0.4);4.5219 (0.6); 4.5075 (0.6); 4.5024 (0.5); 4.4876 (0.4); 3.6687 (12.3);3.3252 (6.8); 2.5765 (0.7); 2.5603 (0.8); 2.5582 (0.8); 2.5499 (0.6);2.5423 (0.6); 2.5302 (1.2); 2.5121 (4.0); 2.5077 (7.3); 2.5031 (9.4);2.4985 (6.9); 2.4940 (3.3); 2.4209 (12.5); 2.0540 (16.0); 2.0445 (1.3);2.0393 (0.8); 2.0300 (0.8); 2.0233 (0.8); 2.0176 (0.5); 2.0112 (0.4);2.0025 (0.4); 1.2384 (0.3); −0.0002 (6.7) I.73: ¹H-NMR(400.2 MHz,d₆-DMSO): δ = 8.6973 (1.1); 8.6777 (1.1); 7.3172 (0.3); 7.3146 (0.5);7.3010 (0.6); 7.2958 (2.6); 7.2946 (2.5); 7.2865 (3.3); 7.2802 (9.7);7.2696 (0.6); 7.2654 (0.9); 7.2365 (0.7); 7.2310 (0.8); 7.2214 (0.7);7.2149 (0.9); 7.2117 (0.5); 7.2065 (0.5); 7.1999 (0.4); 4.6336 (0.4);4.6213 (0.5); 4.6140 (0.5); 4.6073 (0.6); 4.6017 (0.6); 4.5950 (0.5);4.5877 (0.6); 4.5753 (0.4); 3.6676 (16.0); 3.3296 (11.4); 3.2021 (0.7);3.1898 (0.7); 3.1677 (1.1); 3.1554 (1.0); 3.0565 (1.1); 3.0301 (1.1);3.0221 (0.8); 2.9957 (0.7); 2.5121 (3.9); 2.5076 (8.2); 2.5030 (10.8);2.4984 (7.7); 2.4939 (3.7); 2.1967 (15.4); −0.0002 (6.7) I.74:¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.6444 (1.0); 8.6252 (1.0); 4.4023(0.4); 4.3909 (0.5); 4.3830 (0.4); 4.3769 (0.5); 4.3719 (0.6); 4.3647(0.5); 4.3577 (0.4); 4.3454 (0.4); 4.1579 (0.4); 4.1487 (0.5); 4.1400(0.5); 4.1371 (0.7); 4.1309 (1.8); 4.1194 (1.9); 4.1131 (1.9); 4.1017(1.8); 4.0953 (0.7); 4.0927 (0.6); 4.0840 (0.6); 4.0747 (0.4); 3.3277(25.7); 2.5204 (0.5); 2.5119 (6.1); 2.5074 (12.8); 2.5029 (17.2); 2.4983(12.8); 2.4938 (6.4); 2.3735 (16.0); 1.7554 (0.4); 1.7407 (0.4); 1.7350(0.4); 1.7289 (0.6); 1.7234 (0.7); 1.6980 (0.8); 1.6861 (0.5); 1.6822(0.4); 1.6696 (0.5); 1.6654 (0.5); 1.6530 (0.4); 1.6490 (0.4); 1.5908(0.6); 1.5785 (0.5); 1.5691 (0.4); 1.5580 (0.8); 1.5469 (0.5); 1.5370(0.4); 1.2393 (0.4); 1.2108 (4.4); 1.1930 (9.1); 1.1753 (4.2); 0.9281(5.5); 0.9121 (5.3); 0.8924 (5.2); 0.8764 (5.2); −0.0002 (7.9) I.75:¹H-NMR(300.2 MHz, CDCl3): δ = 7.4618 (0.5); 7.4535 (0.9); 7.4487 (0.7);7.4404 (1.6); 7.4274 (4.3); 7.4159 (1.2); 7.4097 (3.3); 7.4075 (3.3);7.4003 (1.1); 7.3918 (1.7); 7.3836 (2.3); 7.3776 (1.2); 7.3640 (0.8);7.2981 (0.5); 6.9778 (0.7); 6.9559 (0.7); 5.7106 (2.2); 5.6880 (2.2);4.3311 (0.6); 4.3191 (0.5); 4.3073 (0.6); 4.2953 (1.4); 4.2713 (1.8);4.2469 (1.8); 4.2230 (1.4); 4.2109 (0.6); 4.1993 (0.5); 4.1872 (0.6);2.5318 (16.0); 1.2899 (4.2); 1.2661 (8.5); 1.2423 (4.1); 0.0395 (0.5)I.76: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.4610 (0.5); 7.4526 (0.8); 7.4484(0.7); 7.4396 (1.7); 7.4266 (4.5); 7.4191 (1.4); 7.4158 (1.4); 7.4097(3.4); 7.4075 (3.2); 7.4001 (1.2); 7.3921 (1.8); 7.3838 (2.2); 7.3644(0.8); 7.2980 (0.6); 6.9659 (0.7); 6.9439 (0.7); 5.7084 (2.2); 5.6858(2.2); 4.3301 (0.6); 4.3182 (0.5); 4.3063 (0.7); 4.2943 (1.4); 4.2703(1.8); 4.2460 (1.8); 4.2221 (1.4); 4.2100 (0.6); 4.1984 (0.5); 4.1862(0.6); 2.5863 (16.0); 1.2899 (4.2); 1.2661 (8.4); 1.2423 (4.0); 0.0392(0.6) I.77: ¹H-NMR(400.1 MHz, CDCl3): δ = 7.2631 (10.2); 6.2910 (1.2);5.0930 (0.4); 5.0824 (0.7); 5.0715 (1.0); 5.0609 (1.4); 5.0504 (1.0);5.0388 (0.7); 5.0302 (0.3); 4.2055 (5.5); 4.1933 (5.4); 3.9529 (1.2);3.9418 (2.2); 3.9248 (1.7); 3.9121 (2.5); 3.9010 (1.4); 3.5810 (1.5);3.5745 (1.7); 3.5517 (2.8); 3.5288 (1.4); 3.5229 (1.4); 2.9579 (1.3);2.8850 (1.2); 2.5625 (16.0); 1.9798 (1.4); 1.9710 (1.5); 1.9590 (1.4);1.9462 (1.9); 1.9388 (1.9); 1.7726 (0.8); 1.7629 (0.9); 1.7502 (1.6);1.7401 (2.1); 1.7290 (1.4); 1.7179 (1.9); 1.7077 (1.2); 1.6958 (0.6);1.6852 (0.6); 1.5625 (7.0); −0.0002 (6.7) I.78: ¹H-NMR(400.1 MHz,CDCl3): δ = 7.2612 (10.3); 6.3202 (1.0); 5.1470 (0.5); 5.1315 (1.2);5.1155 (1.5); 5.1001 (1.2); 5.0845 (0.5); 4.1574 (5.4); 4.1453 (5.3);2.5608 (15.4); 1.5538 (12.7); 1.3017 (16.0); 1.2862 (15.8); −0.0002(5.0) I.79: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.5272 (1.0); 8.5092 (1.0);4.3603 (1.0); 4.3420 (1.6); 4.3238 (1.0); 2.8918 (0.4); 2.7333 (0.3);2.7321 (0.3); 2.5124 (4.4); 2.5079 (8.9); 2.5033 (11.7); 2.4987 (8.3);2.4941 (3.9); 2.4250 (16.0); 1.3709 (6.1); 1.3526 (6.0); −0.0002 (8.9)I.80: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.5409 (0.5); 8.5268 (1.0); 8.5123(0.5); 7.9522 (0.5); 3.8951 (4.0); 3.8805 (4.0); 3.7792 (0.5); 3.6363(1.2); 3.5437 (1.6); 3.3131 (0.5); 2.8944 (3.4); 2.7358 (2.8); 2.7347(2.8); 2.5181 (3.6); 2.5137 (7.4); 2.5091 (9.8); 2.5045 (7.2); 2.5000(3.5); 2.4085 (16.0); −0.0002 (4.1) I.81: ¹H-NMR(400.2 MHz, d₆-DMSO): δ= 8.5222 (0.9); 8.5043 (0.9); 7.9535 (1.9); 4.3621 (1.0); 4.3439 (1.5);4.3257 (1.0); 2.8922 (13.5); 2.7335 (11.5); 2.7324 (11.0); 2.5458 (0.5);2.5211 (0.3); 2.5126 (4.2); 2.5081 (8.4); 2.5035 (11.0); 2.4989 (7.8);2.4944 (3.6); 2.3890 (16.0); 1.3757 (6.0); 1.3574 (5.9); −0.0002 (7.0)I.82: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.3653 (1.0); 8.3452 (1.0); 7.9534(0.4); 4.2186 (1.1); 4.2028 (1.2); 4.1985 (1.2); 4.1827 (1.1); 2.8922(2.8); 2.7336 (2.3); 2.7323 (2.3); 2.5477 (0.5); 2.5211 (0.4); 2.5125(4.6); 2.5080 (9.3); 2.5034 (12.2); 2.4988 (8.8); 2.4943 (4.2); 2.4457(1.1); 2.3771 (16.0); 2.3708 (1.7); 2.1931 (0.5); 2.1763 (0.8); 2.1597(0.8); 2.1429 (0.5); 0.9605 (10.5); 0.9434 (10.2); 0.9305 (0.5); 0.9183(0.4); 0.9143 (0.5); 0.9025 (0.6); 0.8973 (0.4); 0.8862 (0.3); 0.0080(0.3); −0.0002 (8.8) I.83: ¹H-NMR(400.1 MHz, d₆-DMSO): δ = 8.2727 (2.2);8.2525 (2.1); 7.9603 (1.5); 4.4433 (1.6); 4.4275 (2.1); 4.4112 (1.5);3.3334 (18.0); 3.0685 (0.3); 2.8999 (6.7); 2.7406 (6.3); 2.5101 (8.9);2.3781 (16.0); 1.9992 (1.2); 1.9830 (1.6); 1.9674 (1.3); 1.4459 (0.6);1.4294 (1.0); 1.4122 (1.4); 1.3949 (1.3); 1.3786 (0.9); 1.2528 (0.9);1.2359 (1.4); 1.2186 (1.4); 1.2015 (1.1); 1.1829 (0.6); 0.9330 (8.6);0.9156 (12.1); 0.8961 (8.5); 0.8780 (4.0) I.84: ¹H-NMR(400.2 MHz,d₆-DMSO): δ = 8.5037 (1.1); 8.4838 (1.1); 7.9536 (0.7); 4.3579 (0.5);4.3482 (0.4); 4.3427 (0.5); 4.3381 (0.6); 4.3315 (0.5); 4.3232 (0.4);4.3116 (0.4); 2.8924 (4.8); 2.7338 (3.9); 2.7327 (4.1); 2.5475 (0.5);2.5127 (4.9); 2.5083 (10.1); 2.5037 (13.4); 2.4991 (9.7); 2.4946 (4.7);2.4386 (0.8); 2.3790 (16.0); 2.3711 (1.4); 1.7447 (0.4); 1.7289 (0.4);1.7238 (0.4); 1.7174 (0.7); 1.7137 (0.7); 1.6983 (0.5); 1.6870 (0.8);1.6709 (0.5); 1.6663 (0.5); 1.6545 (0.4); 1.6502 (0.4); 1.6027 (0.6);1.5907 (0.4); 1.5809 (0.4); 1.5706 (0.8); 1.5600 (0.4); 0.9239 (5.3);0.9080 (5.2); 0.8901 (5.0); 0.8743 (4.9); −0.0002 (8.0) I.85:¹H-NMR(400.1 MHz, d₆-DMSO): δ = 8.5180 (1.9); 8.4991 (1.9); 7.9602(0.8); 4.4520 (1.4); 4.4400 (1.4); 3.3307 (19.0); 2.8989 (3.5); 2.7400(3.2); 2.5779 (1.5); 2.5580 (2.4); 2.5368 (2.6); 2.5103 (10.0); 2.3957(13.6); 2.0614 (16.0); 2.0039 (0.8); 1.2642 (0.4); 1.2477 (0.4) I.86:¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.5160 (1.3); 8.4958 (1.3); 7.9534(1.4); 7.2874 (7.4); 7.2764 (12.3); 7.2659 (0.7); 7.2241 (0.8); 7.2130(1.2); 7.2024 (1.3); 7.1948 (0.5); 7.1907 (0.7); 4.5618 (0.4); 4.5507(0.5); 4.5414 (0.5); 4.5351 (0.7); 4.5310 (0.6); 4.5244 (0.5); 4.5152(0.5); 4.5041 (0.4); 3.2195 (0.8); 3.2084 (0.9); 3.1850 (1.1); 3.1740(1.0); 3.0347 (1.1); 3.0080 (1.1); 3.0003 (0.9); 2.9736 (0.8); 2.8909(10.4); 2.7331 (8.7); 2.7320 (8.6); 2.5451 (0.6); 2.5209 (0.5); 2.5123(6.5); 2.5078 (13.6); 2.5033 (18.0); 2.4987 (13.0); 2.4941 (6.3); 2.4423(0.5); 2.1912 (16.0); 0.0080 (0.4); −0.0002 (11.9); −0.0085 (0.4) I.87:¹H-NMR(400.1 MHz, d₆-DMSO): δ = 8.5093 (2.0); 8.4904 (2.0); 7.9600(1.2); 4.4403 (1.5); 4.4292 (1.4); 3.5729 (0.4); 3.5582 (0.4); 3.3284(60.1); 3.0720 (0.4); 2.8997 (5.2); 2.7405 (4.9); 2.5733 (1.7); 2.5542(2.8); 2.5106 (17.5); 2.4335 (13.7); 2.0606 (16.0); 1.9943 (1.0); 1.2598(0.5); 1.2435 (0.5) I.88: ¹H-NMR(400.1 MHz, d₆-DMSO): δ = 8.5092 (2.3);8.4901 (2.3); 7.9603 (2.4); 7.2839 (14.4); 7.2212 (2.1); 4.5415 (1.7);3.3304 (51.8); 3.2177 (2.5); 3.1836 (2.6); 3.0679 (0.4); 3.0349 (1.8);3.0061 (2.2); 2.9731 (1.3); 2.8984 (10.5); 2.7397 (10.0); 2.5105 (13.6);2.2400 (16.0) I.89: ¹H-NMR(499.9 MHz, d₆-DMSO): δ = 12.7827 (1.0);8.2866 (2.9); 8.2699 (2.9); 4.4317 (2.5); 4.4215 (2.7); 4.4150 (2.6);4.4047 (2.5); 3.3170 (3.0); 2.5116 (5.3); 2.5081 (11.0); 2.5046 (15.1);2.5010 (11.0); 2.4975 (5.2); 2.4072 (38.2); 1.9991 (0.6); 1.9856 (1.4);1.9731 (1.7); 1.9605 (1.4); 1.9470 (0.7); 1.4296 (0.9); 1.4162 (1.4);1.4020 (2.0); 1.3877 (1.7); 1.3743 (1.2); 1.3597 (0.3); 1.2397 (1.2);1.2249 (2.0); 1.2104 (1.7); 1.1975 (1.6); 1.1827 (1.0); 0.9221 (15.5);0.9083 (15.9); 0.9035 (9.2); 0.8886 (16.0); 0.8738 (6.7) I.90:¹H-NMR(300.2 MHz, d₆-DMSO): δ = 12.7133 (0.7); 8.5333 (2.7); 8.5069(2.8); 4.3890 (0.6); 4.3748 (1.2); 4.3624 (0.9); 4.3484 (1.5); 4.3400(1.2); 4.3284 (0.7); 4.3136 (0.9); 3.3524 (16.0); 2.5339 (5.4); 2.5280(11.2); 2.5219 (15.3); 2.5159 (11.2); 2.5101 (5.4); 2.4326 (33.0);2.0956 (0.3); 1.7793 (0.5); 1.7648 (0.9); 1.7283 (2.0); 1.6984 (1.8);1.6821 (1.5); 1.6639 (1.0); 1.6432 (0.8); 1.6170 (1.5); 1.5912 (0.8);1.5778 (1.5); 1.5638 (0.9); 1.5513 (0.5); 0.9422 (10.2); 0.9217 (10.2);0.9083 (10.3); 0.8876 (10.0); 0.0304 (0.4); 0.0194 (9.8); 0.0083 (0.4)I.91: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.2994 (2.8); 6.3458 (0.5); 6.3191(0.5); 4.7660 (1.2); 4.7507 (1.2); 4.7379 (1.1); 4.7226 (1.1); 3.8211(16.0); 2.5383 (15.5); 2.3377 (0.5); 2.3220 (0.5); 2.3148 (0.7); 2.2994(0.7); 2.2919 (0.6); 2.2765 (0.5); 1.0442 (6.6); 1.0213 (6.6); 1.0101(6.9); 0.9871 (6.5); 0.0350 (0.9) I.92: ¹H-NMR(300.2 MHz, CDCl3): δ =7.2990 (0.8); 6.4532 (1.3); 3.7374 (16.0); 2.5560 (15.5); 1.7066 (1.0);1.7009 (1.2); 1.6839 (3.2); 1.6730 (3.4); 1.6578 (1.4); 1.3263 (1.4);1.3108 (3.4); 1.3001 (3.3); 1.2833 (1.2); 0.0278 (1.0) IVa.01:1H-NMR(300.2 MHz, d6-DMSO): δ = 4.0799 (5.3); 4.0586 (5.4); 3.3415(4.9); 2.5524 (17.9); 2.5343 (0.7); 2.5282 (1.2); 2.5221 (1.7); 2.5160(1.2); 2.5100 (0.6); 2.0454 (0.4); 2.0232 (0.8); 2.0010 (1.0); 1.9789(0.8); 1.9568 (0.4); 1.2627 (0.6); 0.9753 (16.0); 0.9529 (15.3); 0.8761(0.6); 0.0180 (1.3) IVa.02: 1H-NMR(499.9 MHz, CDCl3): δ = 7.2622 (1.9);4.3528 (1.2); 4.3385 (4.0); 4.3242 (4.3); 4.3100 (1.9); 2.5262 (16.0);2.4981 (1.1); 1.3792 (4.2); 1.3650 (8.5); 1.3507 (5.1); 1.3366 (1.2);1.2972 (0.6); 1.2845 (0.7); 1.2536 (5.5); 1.1056 (0.3); 0.8885 (0.6);0.8799 (0.9); 0.8739 (0.8); 0.8656 (0.9); 0.8558 (1.0); 0.8412 (0.9);−0.0002 (1.7) IVa.03: 1H-NMR(400.1 MHz, d6-DMSO): δ = 4.0712 (5.4);4.0552 (5.4); 3.3163 (4.8); 2.5139 (1.6); 2.5096 (2.2); 2.5053 (1.6);2.4861 (17.1); 2.0251 (0.5); 2.0085 (0.9); 1.9919 (1.2); 1.9753 (1.0);1.9587 (0.5); 0.9630 (16.0); 0.9462 (15.5) VIa.01: 1H-NMR(300.2 MHz,CDCl3): δ = 7.7266 (0.9); 7.2983 (1.8); 4.3473 (2.2); 4.3235 (6.6);4.2997 (6.8); 4.2799 (9.4); 4.2639 (8.9); 1.6684 (1.5); 1.3796 (8.0);1.3558 (16.0); 1.3319 (7.7); 0.0290 (2.0) VIa.02: 1H-NMR(300.2 MHz,CDCl3): δ = 7.6832 (0.5); 7.2980 (1.8); 4.3203 (5.0); 4.3043 (4.9);3.8640 (16.0); 1.6217 (0.6); 0.0330 (2.2) VIa.03: 1H-NMR(300.2 MHz,CDCl3): δ = 7.6908 (0.5); 7.2986 (3.4); 4.3181 (4.8); 4.3021 (4.8);3.8644 (16.0); 2.0812 (0.4); 1.6018 (1.6); 0.0358 (4.1) VIa.04:1H-NMR(400.2 MHz, d6-DMSO): δ = 9.0297 (2.9); 4.1005 (2.1); 4.0828(6.7); 4.0651 (6.7); 4.0473 (2.1); 3.3285 (11.9); 2.5220 (0.4); 2.5133(6.0); 2.5088 (12.5); 2.5042 (16.6); 2.4995 (12.0); 2.4950 (5.9); 1.4637(1.8); 1.4515 (4.4); 1.4431 (4.8); 1.4322 (2.0); 1.1946 (2.2); 1.1820(10.0); 1.1753 (4.9); 1.1641 (16.0); 1.1463 (7.1); −0.0002 (0.4) VIa.05:1H-NMR(499.9 MHz, d6-DMSO): δ = 9.1058 (3.8); 4.1569 (2.1); 4.1426(6.5); 4.1284 (6.6); 4.1143 (2.1); 3.3757 (1.0); 2.5650 (0.4); 2.5615(0.8); 2.5579 (1.0); 2.5543 (0.8); 2.5508 (0.4); 1.5126 (1.8); 1.5030(4.7); 1.4964 (5.0); 1.4875 (2.0); 1.2481 (7.1); 1.2338 (16.0); 1.2238(5.6); 1.2196 (9.1); 1.2076 (1.9) VIa.06: 1H-NMR(300.2 MHz, d6-DMSO): δ= 12.5912 (0.3); 12.5704 (0.3); 8.9622 (5.6); 3.3582 (16.0); 2.5348(7.3); 2.5289 (15.6); 2.5228 (21.8); 2.5167 (15.8); 2.5108 (7.3); 1.4582(2.0); 1.4422 (5.0); 1.4314 (5.7); 1.4172 (2.5); 1.1587 (2.6); 1.1445(5.5); 1.1336 (5.4); 1.1178 (2.0); 0.0317 (1.0); 0.0207 (30.4); 0.0098(1.1) VIa.07: 1H-NMR(400.2 MHz, d6-DMSO): δ = 9.0605 (4.1); 8.3150(0.5); 4.1032 (2.2); 4.0855 (7.1); 4.0677 (7.1); 4.0500 (2.3); 3.3287(15.8); 2.8923 (0.7); 2.7326 (0.6); 2.5263 (0.4); 2.5216 (0.6); 2.5128(8.7); 2.5084 (18.0); 2.5038 (23.9); 2.4992 (17.7); 2.4948 (8.9); 1.4546(1.8); 1.4425 (4.6); 1.4343 (5.1); 1.4233 (2.1); 1.1961 (7.7); 1.1783(16.0); 1.1693 (2.6); 1.1604 (9.6); 1.1499 (5.1); 1.1378 (1.8); −0.0002(0.5) VIa.08: 1H-NMR(300.2 MHz, d6-DMSO): δ = 9.0801 (2.6); 3.6446(16.0); 3.3477 (11.1); 2.5279 (2.3); 2.5220 (3.1); 2.5161 (2.2); 1.4960(1.0); 1.4795 (2.8); 1.4685 (3.1); 1.4541 (1.3); 1.2106 (1.4); 1.1961(3.1); 1.1851 (2.9); 1.1685 (1.1); 0.0189 (2.7) VIa.09: 1H-NMR(300.2MHz, d6-DMSO): δ = 12.6292 (0.5); 12.5891 (0.6); 12.5706 (0.6); 12.5368(0.5); 8.9512 (15.1); 6.8906 (0.3); 3.3471 (16.0); 2.5343 (14.3); 2.5283(29.9); 2.5222 (40.7); 2.5161 (28.9); 2.5102 (13.1); 2.2042 (0.5);2.0093 (1.1); 1.9289 (0.4); 1.4951 (0.3); 1.4457 (5.1); 1.4297 (12.6);1.4189 (14.1); 1.4050 (6.2); 1.3753 (4.2); 1.3509 (0.6); 1.2561 (0.6);1.2184 (0.5); 1.2012 (1.5); 1.1949 (1.1); 1.1708 (0.7); 1.1518 (6.7);1.1379 (14.3); 1.1271 (13.5); 1.1112 (5.0); 0.0308 (1.6); 0.0200 (45.4);0.0090 (1.5) VIa.10: 1H-NMR(400.2 MHz, d6-DMSO): δ = 8.7446 (0.8);8.7304 (1.7); 8.7161 (0.8); 4.1608 (2.2); 4.1430 (7.0); 4.1252 (7.1);4.1075 (2.3); 4.0177 (6.3); 4.0032 (6.3); 3.3296 (12.4); 2.8929 (0.6);2.7342 (0.5); 2.7332 (0.5); 2.5270 (0.4); 2.5223 (0.6); 2.5135 (7.2);2.5091 (14.7); 2.5045 (19.2); 2.4999 (13.9); 2.4954 (6.7); 1.2357 (8.0);1.2179 (16.0); 1.2001 (7.6); −0.0002 (0.4) VIa.11: 1H-NMR(400.2 MHz,d6-DMSO): δ = 8.5453 (1.5); 8.5258 (1.5); 4.3175 (1.6); 4.3022 (1.8);4.2980 (1.8); 4.2826 (1.6); 4.2026 (1.0); 4.1934 (0.8); 4.1849 (1.0);4.1757 (2.7); 4.1664 (1.2); 4.1579 (2.9); 4.1485 (2.9); 4.1399 (1.2);4.1308 (2.8); 4.1215 (1.1); 4.1131 (0.9); 4.1037 (1.1); 4.0860 (0.3);3.3279 (12.9); 2.8931 (0.9); 2.7344 (0.7); 2.7330 (0.7); 2.5268 (0.4);2.5221 (0.6); 2.5134 (8.1); 2.5089 (16.5); 2.5043 (21.5); 2.4996 (15.3);2.4951 (7.2); 2.2143 (0.8); 2.1976 (1.2); 2.1813 (1.3); 2.1645 (0.8);1.2379 (7.9); 1.2201 (16.0); 1.2023 (7.4); 0.9932 (9.5); 0.9770 (14.5);0.9607 (8.7); −0.0002 (0.5) VIa.12: 1H-NMR(499.9 MHz, d6-DMS0): δ =8.7100 (1.0); 8.6988 (1.8); 8.6874 (0.9); 4.1628 (2.4); 4.1486 (7.0);4.1343 (7.0); 4.1201 (2.2); 4.0351 (6.9); 4.0236 (6.7); 3.3227 (1.6);2.5139 (0.4); 2.5104 (0.7); 2.5067 (0.9); 2.5031 (0.6); 1.2367 (8.0);1.2224 (16.0); 1.2082 (7.6) VIa.13: 1H-NMR(300.2 MHz, d6-DMSO): δ =8.5980 (0.5); 3.9800 (1.7); 3.9611 (1.7); 3.3447 (16.0); 2.5345 (3.3);2.5285 (7.1); 2.5224 (9.9); 2.5164 (7.2); 2.5104 (3.3); 2.0099 (0.4);0.0317 (0.4); 0.0208 (14.2); 0.0098 (0.5) VIa.14: 1H-NMR(400.2 MHz,d6-DMSO): δ = 8.7570 (1.9); 8.7380 (2.0); 7.3230 (0.9); 7.3202 (1.4);7.3165 (0.6); 7.3022 (4.0); 7.2996 (3.1); 7.2899 (1.2); 7.2846 (5.3);7.2719 (4.3); 7.2678 (6.6); 7.2614 (1.1); 7.2511 (2.6); 7.2465 (2.4);7.2426 (1.6); 7.2375 (0.8); 7.2308 (0.9); 7.2248 (2.4); 7.2178 (0.5);7.2120 (0.5); 7.2075 (0.8); 7.2034 (0.4); 4.6413 (0.6); 4.6273 (0.8);4.6188 (1.1); 4.6081 (1.0); 4.6050 (1.0); 4.5998 (0.9); 4.5857 (0.7);4.1411 (1.5); 4.1235 (4.8); 4.1064 (5.2); 4.0887 (1.8); 3.3294 (20.9);3.1759 (0.9); 3.1620 (1.0); 3.1414 (1.8); 3.1277 (1.6); 3.0775 (1.7);3.0546 (1.7); 3.0431 (1.0); 3.0202 (0.9); 2.8913 (1.0); 2.7333 (0.8);2.7322 (0.8); 2.5258 (0.6); 2.5210 (0.8); 2.5124 (11.3); 2.5080 (22.9);2.5034 (29.8); 2.4988 (21.4); 2.4942 (10.2); 1.1871 (7.6); 1.1693(16.0); 1.1515 (7.3); −0.0002 (0.6) VIa.15: 1H-NMR(400.2 MHz, d6-DMSO):δ = 8.7592 (1.8); 8.7404 (1.9); 4.4041 (0.7); 4.3918 (0.7); 4.3852(0.9); 4.3786 (1.1); 4.3731 (0.9); 4.3669 (0.8); 4.3599 (0.9); 4.3479(0.6); 4.1667 (0.6); 4.1575 (1.0); 4.1488 (0.8); 4.1459 (1.2); 4.1397(3.2); 4.1282 (3.4); 4.1219 (3.4); 4.1104 (3.3); 4.1041 (1.3); 4.1015(1.0); 4.0927 (1.0); 4.0835 (0.7); 3.3280 (13.4); 2.8930 (1.0); 2.7334(0.9); 2.5267 (0.4); 2.5219 (0.6); 2.5132 (9.0); 2.5088 (18.2); 2.5043(23.9); 2.4997 (17.3); 2.4952 (8.4); 1.7758 (0.5); 1.7706 (0.5); 1.7624(0.8); 1.7563 (1.1); 1.7469 (1.5); 1.7284 (1.2); 1.7211 (1.6); 1.7085(0.8); 1.6956 (1.1); 1.6830 (0.8); 1.6100 (0.6); 1.6055 (0.5); 1.5938(1.0); 1.5838 (0.9); 1.5721 (1.6); 1.5606 (0.8); 1.5480 (0.4); 1.5380(0.5); 1.2249 (7.8); 1.2072 (16.0); 1.1894 (7.5); 0.9325 (9.4); 0.9165(9.4); 0.9040 (9.2); 0.8879 (8.8); −0.0002 (0.5) VIa.16: 1H-NMR(400.2MHz, d6-DMSO): δ = 8.8160 (1.0); 8.7974 (1.0); 4.5250 (0.4); 4.5112(0.5); 4.5045 (0.7); 4.4913 (0.6); 4.4853 (0.5); 4.4715 (0.4); 4.1686(0.5); 4.1583 (0.7); 4.1508 (1.6); 4.1404 (1.7); 4.1329 (1.7); 4.1227(1.6); 4.1146 (0.7); 4.1049 (0.5); 3.3280 (6.7); 2.6263 (0.7); 2.6105(1.3); 2.5910 (1.7); 2.5721 (0.7); 2.5662 (0.4); 2.5566 (0.6); 2.5128(4.9); 2.5084 (9.7); 2.5039 (12.6); 2.4993 (9.2); 2.4949 (4.5); 2.0655(16.0); 2.0549 (1.0); 2.0455 (0.9); 2.0413 (0.8); 2.0300 (0.7); 2.0253(0.6); 2.0095 (0.4); 1.2317 (3.8); 1.2242 (0.6); 1.2139 (7.7); 1.1961(3.6) VIa.17: 1H-NMR(400.2 MHz, d6-DMSO): δ = 8.4679 (1.4); 8.4484(1.4); 4.3306 (1.8); 4.3155 (2.0); 4.3111 (2.0); 4.2960 (1.8); 4.2263(0.3); 4.2085 (1.1); 4.1993 (0.9); 4.1908 (1.1); 4.1815 (2.9); 4.1701(1.1); 4.1637 (3.0); 4.1523 (3.0); 4.1460 (1.1); 4.1346 (3.0); 4.1253(1.2); 4.1169 (0.9); 4.1076 (1.1); 4.0898 (0.4); 3.3272 (13.7); 2.5269(0.4); 2.5222 (0.6); 2.5135 (7.8); 2.5091 (15.6); 2.5045 (20.3); 2.4999(14.6); 2.4954 (7.0); 2.2189 (0.9); 2.2021 (1.4); 2.1861 (1.4); 2.1693(0.9); 1.2350 (8.1); 1.2172 (16.0); 1.1995 (7.6); 0.9813 (10.9); 0.9679(12.2); 0.9644 (12.1); 0.9509 (10.0); −0.0002 (0.4) VIa.18: 1H-NMR(400.2MHz, d6-DMSO): δ = 8.7118 (1.5); 8.6928 (1.5); 4.4275 (0.5); 4.4158(0.9); 4.4087 (0.7); 4.4029 (0.8); 4.3968 (1.0); 4.3907 (0.9); 4.3840(0.6); 4.3717 (0.7); 4.1696 (0.6); 4.1605 (1.0); 4.1500 (1.2); 4.1427(3.1); 4.1322 (3.3); 4.1248 (3.3); 4.1144 (3.2); 4.1069 (1.2); 4.0968(1.0); 4.0874 (0.6); 3.3279 (16.2); 2.8936 (1.4); 2.7345 (1.2); 2.7333(1.1); 2.5269 (0.4); 2.5221 (0.6); 2.5134 (7.8); 2.5090 (15.8); 2.5044(20.5); 2.4997 (14.6); 2.4952 (6.9); 1.7756 (0.5); 1.7632 (0.8); 1.7497(0.5); 1.7377 (1.5); 1.7310 (1.5); 1.7139 (1.9); 1.7012 (1.0); 1.6850(0.4); 1.6146 (0.7); 1.6003 (0.8); 1.5888 (1.5); 1.5772 (0.8); 1.2332(0.3); 1.2201 (7.7); 1.2024 (16.0); 1.1846 (7.4); 0.9318 (8.4); 0.9160(8.0); 0.9001 (8.0); 0.8841 (7.6); −0.0002 (0.4) VIa.19: 1H-NMR(400.2MHz, d6-DMSO): δ = 8.7776 (0.7); 8.7591 (0.8); 4.5404 (0.4); 4.5346(0.6); 4.5210 (0.5); 4.5154 (0.4); 4.5011 (0.3); 4.1724 (0.4); 4.1634(0.7); 4.1545 (1.5); 4.1454 (1.7); 4.1367 (1.6); 4.1277 (1.5); 4.1187(0.8); 4.1100 (0.5); 3.3275 (6.3); 2.8934 (0.8); 2.7345 (0.7); 2.7331(0.7); 2.6019 (0.6); 2.5865 (1.1); 2.5834 (0.9); 2.5671 (1.6); 2.5518(0.4); 2.5487 (0.6); 2.5134 (3.5); 2.5088 (7.0); 2.5042 (9.2); 2.4996(6.6); 2.4950 (3.2); 2.0904 (0.4); 2.0854 (0.4); 2.0764 (0.5); 2.0714(0.9); 2.0602 (16.0); 2.0491 (0.8); 2.0451 (0.6); 2.0389 (0.4); 2.0286(0.4); 1.2275 (3.7); 1.2189 (0.3); 1.2098 (7.6); 1.1920 (3.5) VIa.20:1H-NMR(400.2 MHz, d6-DMS0): δ = 8.6332 (1.6); 8.6144 (1.6); 7.3226(0.8); 7.3198 (1.3); 7.3160 (0.6); 7.3018 (3.7); 7.2993 (3.2); 7.2900(1.2); 7.2843 (5.4); 7.2746 (4.6); 7.2706 (6.8); 7.2641 (1.0); 7.2541(2.4); 7.2498 (1.4); 7.2465 (1.6); 7.2428 (1.5); 7.2374 (0.8); 7.2312(0.9); 7.2251 (2.3); 7.2180 (0.5); 7.2128 (0.5); 7.2080 (0.8); 7.2038(0.4); 4.6760 (0.7); 4.6622 (0.9); 4.6569 (1.0); 4.6537 (1.2); 4.6432(1.0); 4.6401 (1.0); 4.6348 (1.0); 4.6209 (0.7); 4.1481 (1.5); 4.1317(4.6); 4.1304 (4.6); 4.1138 (5.0); 4.0959 (1.7); 3.3305 (17.0); 3.2003(0.9); 3.1866 (1.0); 3.1658 (1.8); 3.1522 (1.7); 3.1031 (1.8); 3.0805(1.8); 3.0687 (1.0); 3.0461 (1.0); 2.8916 (1.0); 2.7338 (0.8); 2.7327(0.9); 2.5264 (0.4); 2.5216 (0.6); 2.5129 (8.5); 2.5085 (17.0); 2.5039(22.1); 2.4993 (15.9); 2.4947 (7.6); 1.1861 (7.7); 1.1684 (16.0); 1.1506(7.4); −0.0002 (0.4) VIa.21: 1H-NMR(400.2 MHz, d6-DMSO): δ = 8.5103(1.4); 8.4908 (1.4); 4.3318 (1.4); 4.3166 (1.7); 4.3124 (1.6); 4.2971(1.4); 4.2063 (0.8); 4.1970 (0.7); 4.1885 (0.8); 4.1793 (2.2); 4.1704(1.0); 4.1615 (2.3); 4.1526 (2.3); 4.1436 (1.0); 4.1348 (2.3); 4.1256(0.8); 4.1171 (0.7); 4.1078 (0.8); 3.3229 (19.1); 2.5250 (0.5); 2.5117(10.5); 2.5073 (21.4); 2.5028 (28.2); 2.4983 (20.2); 2.4938 (9.7);2.2231 (0.7); 2.2063 (1.2); 2.1900 (1.2); 2.1733 (0.8); 1.2391 (6.6);1.2214 (13.0); 1.2036 (6.0); 0.9988 (8.7); 0.9816 (16.0); 0.9643 (8.0);−0.0002 (5.3) VIa.22: 1H-NMR(400.2 MHz, d6-DMSO): δ = 8.7477 (2.1);8.7289 (2.1); 4.4118 (0.8); 4.3994 (0.8); 4.3928 (1.0); 4.3867 (1.2);4.3809 (0.9); 4.3749 (0.8); 4.3680 (1.0); 4.3560 (0.6); 4.1690 (0.6);4.1597 (1.0); 4.1486 (1.3); 4.1420 (3.2); 4.1308 (3.4); 4.1242 (3.4);4.1131 (3.2); 4.1062 (1.3); 4.0954 (1.0); 4.0861 (0.6); 3.3229 (26.7);2.5250 (0.7); 2.5113 (14.8); 2.5070 (30.5); 2.5026 (40.5); 2.4981(29.6); 2.4937 (14.6); 1.7949 (0.3); 1.7786 (0.6); 1.7621 (1.3); 1.7531(1.4); 1.7303 (2.0); 1.7178 (0.9); 1.7047 (1.3); 1.6920 (0.8); 1.6176(0.6); 1.6015 (1.0); 1.5916 (0.9); 1.5799 (1.7); 1.5684 (0.8); 1.5549(0.4); 1.5458 (0.5); 1.2389 (0.7); 1.2251 (7.8); 1.2074 (16.0); 1.1896(7.6); 0.9345 (9.8); 0.9186 (9.9); 0.9051 (9.7); 0.8891 (9.4); −0.0002(7.2) VIa.23: 1H-NMR(400.2 MHz, d6-DMSO): δ = 8.8083 (1.0); 8.7898(1.0); 4.5337 (0.3); 4.5137 (0.6); 4.4998 (0.6); 4.4947 (0.5); 4.4804(0.3); 4.1713 (0.5); 4.1613 (0.6); 4.1535 (1.5); 4.1433 (1.6); 4.1356(1.6); 4.1256 (1.5); 4.1174 (0.7); 4.1079 (0.5); 3.3232 (10.4); 2.6291(0.7); 2.6137 (1.3); 2.5945 (1.7); 2.5761 (0.7); 2.5613 (0.3); 2.5115(6.4); 2.5071 (13.2); 2.5026 (17.5); 2.4981 (12.8); 2.4937 (6.3); 2.0813(0.5); 2.0662 (16.0); 2.0485 (0.8); 2.0389 (0.8); 2.0304 (0.4); 2.0185(0.4); 1.2323 (3.7); 1.2146 (7.5); 1.1968 (3.5); −0.0002 (3.4) VIa.24:1H-NMR(400.2 MHz, d6-DMSO): δ = 8.7327 (2.0); 8.7139 (2.0); 7.3206(1.4); 7.3025 (4.2); 7.2902 (1.4); 7.2847 (5.6); 7.2683 (7.1); 7.2515(2.8); 7.2471 (2.6); 7.2432 (1.8); 7.2312 (1.0); 7.2254 (2.4); 7.2187(0.5); 7.2126 (0.5); 7.2082 (0.8); 4.6559 (0.7); 4.6418 (1.0); 4.6337(1.2); 4.6227 (1.1); 4.6199 (1.1); 4.6146 (1.0); 4.6006 (0.7); 4.1446(1.6); 4.1374 (0.3); 4.1271 (5.3); 4.1096 (5.6); 4.0996 (0.3); 4.0919(1.9); 3.3249 (32.0); 3.1832 (1.0); 3.1692 (1.1); 3.1487 (2.0); 3.1349(1.8); 3.0878 (1.9); 3.0651 (1.9); 3.0534 (1.1); 3.0307 (1.0); 2.8912(0.4); 2.7321 (0.3); 2.5246 (0.8); 2.5113 (17.7); 2.5070 (35.1); 2.5025(45.5); 2.4979 (32.5); 2.4935 (15.5); 1.2389 (0.6); 1.1887 (7.7); 1.1709(16.0); 1.1532 (7.4); −0.0002 (7.0) VIIIa.01: 1H-NMR(499.9 MHz, CDCl3):δ = 7.2672 (1.2); 4.4055 (2.5); 4.3912 (7.7); 4.3769 (7.8); 4.3627(2.6); 2.0088 (0.9); 1.4065 (8.0); 1.3922 (16.0); 1.3780 (8.0); 1.2628(0.4); 1.2538 (1.0); −0.0002 (1.4) VIIIa.02: 1H-NMR(300.2 MHz, CDCl3): δ= 7.6041 (0.4); 7.2984 (2.1); 3.9506 (16.0); 3.9244 (1.2); 1.5852 (1.8);0.0364 (2.4) VIIIa.03: 1H-NMR(499.9 MHz, d6-DMSO): δ = 15.1027 (0.3);14.9975 (0.4); 14.9759 (0.4); 14.9509 (0.4); 14.9312 (0.4); 14.8896(0.4); 14.8671 (0.5); 14.8450 (0.5); 14.7865 (0.6); 14.7539 (0.7);14.6142 (1.0); 14.5943 (1.2); 14.5485 (1.4); 14.5271 (1.5); 14.5236(1.5); 14.2968 (4.7); 14.1541 (7.0); 14.0699 (5.8); 13.9449 (3.2);13.8394 (2.0); 13.5699 (0.8); 13.5440 (0.8); 13.4921 (0.6); 13.4731(0.6); 13.4502 (0.6); 13.4216 (0.6); 13.3628 (0.5); 13.3451 (0.5);13.3306 (0.4); 13.2703 (0.5); 13.2252 (0.4); 13.2010 (0.4); 13.1591(0.4); 13.1269 (0.3); 13.0464 (0.3); 7.7544 (8.9); 7.4284 (1.4); 4.5359(0.3); 4.4060 (0.3); 4.3940 (0.3); 4.3632 (0.4); 4.3500 (0.4); 4.3401(0.4); 4.2742 (0.4); 4.2369 (0.4); 4.2278 (0.5); 4.2094 (0.5); 4.1782(0.5); 4.1293 (0.5); 4.1189 (0.6); 4.1132 (0.6); 4.1025 (0.6); 4.0515(0.6); 4.0446 (0.7); 4.0191 (0.7); 3.9836 (0.8); 3.9763 (0.8); 3.9301(0.9); 3.8612 (1.0); 3.4109 (6.4); 3.3496 (7.0); 3.1621 (3.7); 2.8672(1.0); 2.8488 (1.0); 2.8394 (0.9); 2.8120 (0.8); 2.8052 (0.8); 2.7588(0.9); 2.7233 (0.7); 2.7027 (0.7); 2.6458 (1.7); 2.6421 (2.1); 2.6172(0.7); 2.5952 (0.7); 2.5818 (0.7); 2.5143 (96.0); 2.5108 (196.0); 2.5072(264.8); 2.5037 (189.8); 2.5002 (88.3); 2.3720 (1.1); 2.3683 (1.6);2.3644 (1.2); 2.1856 (0.5); 2.0896 (16.0); 2.0780 (0.4); 1.9135 (0.5);1.3579 (3.0); 1.3421 (1.0); 1.3177 (0.4); 1.3006 (1.0); 1.2736 (0.5);1.2600 (1.1); 1.2307 (1.5); 1.2053 (0.4); 1.1833 (2.4); 1.1716 (1.1);1.0969 (0.4); 0.8541 (0.5) VIIIa.04: 1H-NMR(499.9 MHz, d6-DMSO): δ =3.8598 (16.0); 3.3560 (0.5); 2.5322 (0.6); 2.5288 (1.2); 2.5253 (1.7);2.5217 (1.2); 2.5184 (0.6) VIIIa.05: 1H-NMR(300.2 MHz, CDCl3): δ =7.2983 (1.3); 3.9521 (16.0); 1.5875 (0.4); 0.0350 (1.7) VIIIa.06:1H-NMR(300.2 MHz, d6-DMSO): δ = 19.6514 (1.2); 19.4242 (1.2); 14.4211(1.5); 14.2144 (4.5); 14.0488 (9.5); 13.9419 (4.6); 13.7837 (1.7);13.6736 (1.2); 13.6487 (1.2); 13.5662 (1.3); 9.3511 (1.3); 5.7749 (3.0);4.0838 (1.6); 4.0599 (3.6); 4.0367 (3.6); 4.0129 (1.4); 3.7199 (1.5);3.6986 (1.4); 3.6881 (1.6); 3.6447 (2.0); 3.5905 (2.2); 3.5604 (2.8);3.3605 (11.6); 3.1076 (1.9); 3.0934 (1.9); 3.0852 (2.0); 3.0078 (1.6);2.9717 (1.3); 2.9121 (1.4); 2.8858 (1.6); 2.7479 (1.7); 2.5339 (95.7);2.5278 (198.8); 2.5217 (271.4); 2.5157 (195.8); 2.5096 (91.8); 2.4429(1.8); 2.4204 (1.3); 2.2912 (2.1); 2.0080 (16.0); 1.2510 (7.5); 1.2177(5.6); 1.1940 (10.0); 1.1702 (5.6); 0.8674 (1.7); 0.8481 (1.5); 0.8110(1.2); 0.0286 (13.0); 0.0178 (337.9); 0.0069 (13.0); −0.0500 (1.4);−0.1807 (1.7) VIIIa.07: 1H-NMR(499.9 MHz, CDCl3): δ = 7.2630 (2.8);4.4029 (2.5); 4.3887 (7.6); 4.3744 (7.7); 4.3601 (2.6); 2.0073 (0.6);1.5552 (2.0); 1.4026 (8.0); 1.3883 (16.0); 1.3740 (7.8); 1.2543 (0.5);−0.0002 (3.2) VIIIa.08: 1H-NMR(499.9 MHz, CDCl3): δ = 7.2606 (15.4);5.2995 (3.1); 4.3996 (2.5); 4.3853 (7.7); 4.3710 (7.8); 4.3568 (2.6);1.5458 (28.2); 1.3998 (8.0); 1.3856 (16.0); 1.3713 (7.9); 1.2560 (0.6);−0.0002 (15.9) IXb.01: 1H-NMR(300.2 MHz, CDCl3): δ = 7.3562 (4.5);7.2987 (4.8); 6.3762 (1.1); 4.2401 (1.4); 4.2163 (4.4); 4.1925 (4.5);4.1688 (1.5); 2.5394 (16.0); 1.7118 (1.3); 1.6952 (3.6); 1.6843 (3.8);1.6692 (1.7); 1.6163 (0.3); 1.3412 (1.7); 1.3261 (3.7); 1.3153 (3.7);1.2979 (6.0); 1.2740 (9.6); 1.2502 (4.6); 0.0354 (6.2) IXa.01:1H-NMR(600.1 MHz, d6-DMSO): δ = 8.6444 (2.5); 8.3131 (4.9); 7.1174(6.0); 4.0758 (1.6); 4.0640 (5.0); 4.0522 (5.0); 4.0404 (1.6); 3.3303(5.5); 3.3257 (16.0); 3.3238 (13.3); 3.3012 (1.6); 2.5080 (5.1); 2.5052(10.5); 2.5022 (14.0); 2.4993 (9.8); 2.4967 (4.5); 2.3608 (18.4); 2.1549(0.4); 1.4162 (1.5); 1.4084 (3.9); 1.4029 (4.2); 1.3955 (1.6); 1.2397(0.5); 1.1588 (5.3); 1.1469 (11.0); 1.1405 (1.8); 1.1350 (7.0); 1.1276(3.7); 1.1196 (1.3) IXa.02: 1H-NMR(600.1 MHz, d6-DMSO): δ = 8.3748(0.6); 8.3652 (1.2); 8.3555 (0.6); 7.1387 (5.8); 4.1343 (1.6); 4.1225(5.0); 4.1106 (5.0); 4.0988 (1.6); 3.9322 (5.2); 3.9224 (5.2); 3.3259(16.0); 2.8913 (0.4); 2.5081 (4.3); 2.5052 (9.3); 2.5021 (12.9); 2.4991(9.2); 2.4961 (4.2); 2.3919 (18.2); 2.1680 (0.4); 1.2393 (0.5); 1.2146(5.6); 1.2100 (0.3); 1.2027 (11.6); 1.1981 (0.6); 1.1909 (5.5) IXa.03:1H-NMR(600.1 MHz, d6-DMSO): δ = 8.2288 (0.6); 8.2159 (0.6); 7.1279(2.7); 7.1274 (2.6); 4.1797 (0.7); 4.1717 (0.6); 4.1677 (1.1); 4.1599(0.6); 4.1547 (1.0); 4.1538 (1.1); 4.1418 (0.9); 4.1131 (0.9); 4.1013(0.9); 4.0951 (0.5); 4.0832 (0.5); 3.3309 (5.8); 3.3227 (16.0); 2.8917(0.5); 2.7326 (0.4); 2.7318 (0.4); 2.5081 (2.6); 2.5051 (5.9); 2.5020(8.3); 2.4990 (6.1); 2.4960 (3.0); 2.3704 (8.8); 2.1646 (0.4); 2.1532(0.6); 2.1418 (0.6); 2.1304 (0.4); 1.2129 (2.9); 1.2010 (6.0); 1.1957(0.4); 1.1892 (2.8); 0.9602 (3.8); 0.9489 (3.8); 0.9372 (3.7); 0.9259(3.7) IXa.04: 1H-NMR(600.1 MHz, d6-DMSO): δ = 8.3807 (0.4); 8.3678(0.4); 7.2942 (1.0); 7.2836 (2.3); 7.2809 (1.8); 7.2706 (0.3); 7.2189(0.4); 7.0902 (1.6); 4.1169 (0.7); 4.1141 (0.7); 4.1050 (0.7); 4.1023(0.7); 3.3462 (5.2); 3.3412 (15.2); 3.3404 (16.0); 3.1372 (0.4); 3.1285(0.3); 3.0677 (0.4); 3.0507 (0.4); 2.5147 (1.5); 2.5118 (3.3); 2.5088(4.6); 2.5058 (3.4); 2.5029 (1.6); 2.2220 (4.5); 1.1714 (1.4); 1.1596(3.0); 1.1478 (1.4) Xa.01: 1H-NMR(300.2 MHz, d6-DMSO): δ = 8.1387(1.3);6.3153(1.9); 4.0968(0.6); 4.0731(2.1); 4.0495(2.1); 4.0259(0.7);3.3400(16.0); 2.5351(0.6); 2.5291(1.4); 2.5230(1.9); 2.5169(1.4);2.5108(0.6); 2.3046(7.5); 1.4114(0.5); 1.3953(1.2); 1.3843(1.4);1.3703(0.6); 1.1820(2.2); 1.1583(4.8); 1.1347(2.2); 1.1258(0.7);1.1115(1.4); 1.1005(1.3); 1.0842(0.5); 0.0217(1.9) XIa.01: 1H-NMR(300.2MHz, CDCl3): δ = 7.2987 (3.5); 6.2815 (0.7); 4.2225 (0.6); 4.1988 (2.1);4.1750 (2.1); 4.1513 (0.7); 3.8296 (0.9); 3.4388 (1.6); 2.8084 (2.5);2.5446 (1.6); 2.5326 (7.3); 1.6725 (0.7); 1.6561 (1.6); 1.6453 (1.6);1.6302 (0.8); 1.5840 (16.0); 1.2824 (2.2); 1.2587 (4.7); 1.2501 (1.4);1.2350 (2.6); 1.2229 (0.5); 0.0341 (3.4) XIIIa.01: 1H-NMR(499.9 MHz,d6-DMSO): δ = 4.2571 (0.5); 4.2430 (1.6); 4.2288 (1.6); 4.2146 (0.5);3.3173 (2.7); 2.5080 (0.7); 2.5046 (1.0); 2.5012 (0.8); 2.4380 (5.9);1.4974 (16.0); 1.2924 (1.6); 1.2782 (3.4); 1.2640 (1.7) XIIIa.02:1H-NMR(499.9 MHz, d6-DMSO): δ = 3.3167 (18.1); 2.5081 (8.0); 2.5046(11.3); 2.5011 (8.8); 2.4215 (5.9); 1.4920 (16.0); 1.2394 (1.8)

BIOLOGICAL DATA Example A: Xanthomonas Campestris pv. Campestris InVitro Cell Test

Solvent: DMSO

Culture medium: LB broth medium (Luria Broth Miller) Sigma

Inoculum: bacteria suspension

Compounds to be tested were solubilized in DMSO and the solution used toprepare the required range of concentrations. The final concentration ofDMSO used in the assay was ≤1%.

Inoculum was prepared from a pre-culture of bacteria grown in liquidmedium and diluted to the desired optical density (OD).

Compounds were evaluated for their ability to inhibit bacteria growth inliquid culture assay. The compounds were added in the desiredconcentrations to culture medium containing the bacteria suspension.After 24 h of incubation, the efficacy of compounds was determined byspectrometric measurement of bacteria growth. Inhibition was determinedby comparing the absorbance values in wells containing the compoundswith the absorbance in control wells without compounds.

In this test, the following compounds according to the invention showedno direct activity at a concentration of 20 ppm of tested compound:I.01; I.02; I.03; I.04; I.05; I.06; I.07; I.08; I.09; I.10; I.11; I.12;I.13; I.14; I.15; I.17; I.18; I.19; I.20; I.21; I.22; I.23; I.24; I.25;I.26; I.27; I.28; I.29; I.30; I.31; I.32; I.33; I.34; I.35; I.36; I.37;I.38; I.39; I.40; 1.41; I.42; I.43; I.44; I.45; I.46; I.47; I.48; I.49;I.50; 1.51; I.52; 1.53; 1.54; I.55; I.56; I.57; I.58; I.59; 1.60; 1.61.

Example B: In Vivo Preventive Test on Xanthomonas campestris pv.Campestris (Black Rot on Cabbage)

The tested compounds were prepared by homogenization in a mixture ofacetone/Dimethyl sulfoxide/Tween®, and then diluted with water to obtainthe desired concentration.

The young plants of cabbage were treated by spraying the compoundprepared as described above. Control plants were treated only with anaqueous solution of acetone/Dimethyl sulfoxide/Tween®.

After 72 hours, the plants were contaminated by spraying the leaves withan aqueous bacteria suspension of Xanthomonas campestris pv. campestris.The contaminated cabbage plants were incubated for 8 or 10 days at 27°C. at 95% relative humidity.

The test was evaluated 8 or 10 days after the inoculation. 0% means anefficacy which corresponds to that of the control plants while anefficacy of 100% means that no disease was observed.

In this test, the following compounds according to the invention showedefficacy between 70% and 79% at a concentration of 31 ppm of testedcompound: I.08; I.11; I.32; I.34; I.44; I.45; I.50; I.59; I.60; I.68;I.74; I.79; I.80; I.81; I.82; I.90; I.58.

In this test, the following compounds according to the invention showedefficacy between 80% and 89% at a concentration of 31 ppm of testedcompound: I.02; I.15; I.16; I.20; I.25; I.33; I.36; I.40; I.42; I.43;I.52; I.53; I.57.

In this test, the following compounds according to the invention showedefficacy between 90% and 100% at a concentration of 31 ppm of testedcompound: I.03; I.04; I.21; I.31; I.41; I.55; I.56.

Example C: Comparative Examples

Compounds CMP3, CMP4, CMP5 and CMP6 were tested in an in vivo preventivetest on Xanthomonas campestris pv. campestris (black rot on cabbage) inthe same conditions as described in Example B.

Compounds CMP3, CMP4, CMP5 and CMP6 were prepared in accordance with theteaching of U.S. Pat. No. 5,534,541.

The results are as shown in the table below.

Ex. R¹ R² R³ R⁴ R⁵ R⁶ Efficacy (%) CMP3* Br Br Br isopropyl H Et   33I.04 Br Br Me isopropyl H Et >90 CMP4 Br Br H H H Et    0 I.02 Br Br MeH H Et >80 CMP5* Br Br H methyl H H    0 I.79 Br Br Me methyl H H >70CMP6* Br Br H 2-methylpropyl H H   15 I.90 Br Br Me 2-methylpropyl HH >70 *S enantiomer

Example D: Induction of Defense Gene Expression in Arabidopsis thaliana

Arabidopsis thaliana reporter plants containing the coding sequence of agreen fluorescent protein (GFP) linked to the salicylate responsivepromoter sequence of the PR1 (pathogenesis-related protein I) gene(AT2G14610) were grown for five days and then sprayed with compounds. Onthe 3^(rd) day after spraying, plant fluorescence was assessed with aMacroFluo instrument from Leica Microsystems (Wetzlar, Germany).Fluorescences were quantified with the Meta-Morph Microscopy Automation& Image Analysis Software (Molecular Devices, Sunnyvale, Calif., UnitedStates).

Background fluorescence in mock treated leaves was set as 1.00.Salicylic acid treatment (300 ppm) resulted in a relative fluorescencevalue of 2.70, proving the validity of the test system.

In this test, the following compounds according to the invention showeda relative fluorescence value at least above 2 at a concentration of 300ppm of compound: I.01; I.03; I.04; I.05; I.06; I.07; I.08; I.09; I.11;I.13; I.16; I.19; I.20; I.21; I.23; I.24; I.26; I.29; I.30; I.32; I.33;I.35; I.36; I.37; I.39; I.43; I.46; I.47; I.48; I.49; I.50; I.51; I.52;I.53; I.54; I.55; I.57; I.58; I.59; I.60; I.61; I.63; I.64; I.65; I.66;I.67; I.68; I.71; I.72; I.73; I.75; I.76; I.77; I.78; I.79; I.80; I.81;I.82; I.83; I.84; I.85; I.86; I.87; I.88; I.89; I.90; I.91.

In this test, the following compounds according to the invention showeda relative fluorescence value at least above 2 at a concentration of 75ppm of compound: I.02; I.10; I.18; I.25; I.27; I.31; I.34; I.40; I.41;I.56; I.69; I.70; I.15; I.22.

Salicylate is a major defense hormone against plant pathogens. All thecompounds described above stimulate the salicylic acid pathway andtherefore could protect plants against a wide range of pathogens.

The invention claimed is:
 1. A compound of formula (I):

wherein R¹ and R² are identical and are a chlorine atom or a bromineatom; R³ is methyl; R⁴ is selected from the group consisting of hydrogenatom, C₁-C₆-alkyl, aralkyl, aralkyl substituted by hydroxyl, C₁-C₆-alkylsubstituted by a C₁-C₆-alkylsulfanyl and R⁵ is a hydrogen atom; or R⁴and R⁵ form, together with the carbon atom to which they are linked, acyclopropyl; R⁶ is selected from the group consisting of hydrogen atom,C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-cyanoalkyl, C₂-C₆-alkenyl,C₂-C₆-alkynyl, C₃-C₈-cycloalkyl, aryl, aralkyl, 4-, 5- or 6-memberedheterocyclyl, —C₁-C₆-alkyl-Si(C₁-C₆-alkyl)₃ and—C₁-C₆-alkyl-C₃-C₈-cycloalkyl.
 2. The compound of formula (I) accordingto claim 1 wherein R⁴ is selected from the group consisting of hydrogenatom, C₁-C₆-alkyl, benzyl, benzyl substituted by hydroxyl, C₁-C₆-alkylsubstituted by a C₁-C₆-alkylsulfanyl and R⁵ is a hydrogen atom; or R⁴and R⁵ form, together with the carbon atom to which they are linked, acyclopropyl.
 3. The compound of formula (I) according to claim 1 whereinR⁶ is selected from the group consisting of hydrogen atom, C₁-C₆-alkyl,C₁-C₆-haloalkyl, C₁-C₆-cyanoalkyl, C₂-C₆-alkenyl, C₂-C₆-alkynyl,C₃-C₈-cycloalkyl, phenyl, benzyl, 4-, 5- or 6-membered heterocyclyl,—C₁-C₆-alkyl-Si(C₁-C₆-alkyl)₃ and —C₁-C₆-alkyl-cyclopropyl.
 4. Thecompound of formula (I) according to claim 1 wherein R⁶ is selected fromthe group consisting of hydrogen atom, C₁-C₆-alkyl, C₁-C₆-haloalkyl,C₁-C₆-cyanoalkyl, C₂-C₆-alkenyl, C₂-C₆-alkynyl, C₃-C₈-cycloalkyl,phenyl, benzyl, oxetanyl, thietanyl, dioxothietanyl, oxolanyl, oxanyl,—C₁-C₆-alkyl-Si(C₁-C₆-alkyl)₃ and —C₁-C₆-alkyl-cyclopropyl.
 5. Acomposition comprising at least one compound of formula (I) according toclaim 1 and at least one agriculturally suitable auxiliary.
 6. A methodfor controlling bacterial diseases comprising the step of applying (i)at least one compound of formula (I) according to claim 1, or (ii) acomposition comprising at least one compound of formula (I) according toclaim 1 and at least one agriculturally suitable auxiliary to plants,plant parts, seeds, fruits or to the soil in which the plants grow.
 7. Aprocess for preparing a compound of formula (I) according to claim 1comprising the step of reacting a compound of formula (IV) or a saltthereof with a compound of formula (V) or a salt thereof:

wherein R¹, R², R³, R⁴, R⁵ and R⁶ are as recited in claim 1; U¹ is ahalogen atom, a hydroxy group or a C₁-C₆-alkoxy group.
 8. A process forpreparing a compound of formula (I) according to claim 1 comprising thestep of reacting a compound of formula (VI) or a salt thereof with acompound of formula (VII) or a salt thereof:

wherein R¹, R², R³, R⁴, R⁵ and R⁶ are as recited in claim 1; U² is abromine atom, an iodine atom, a mesylate group, a tosylate group or atriflate group; and U³ is a boron derivative or a halogenometal;provided that when R¹ and R² are bromine atoms, U² is not a bromineatom.
 9. The process according to claim 8 further comprising the step ofreacting a compound of formula (VIII):

wherein R¹, R² and U² are as recited in claim 8; and U¹ is a halogenatom, a hydroxy group or a C₁-C₆-alkoxy group, with a compound offormula (V):

wherein R⁴, R⁵ and R⁶ are as defined in claim 8, to provide a compoundof formula (VI).
 10. A process for preparing a compound of formula (I)according to claim 1 comprising the step of performing a bromination orchlorination of a compound of formula (IX) or a salt thereof:

wherein R¹, R², R³, R⁴, R⁵ and R⁶ are as recited in claim 1; U⁴ is ahydrogen atom, a chlorine atom or a bromine atom; and U⁵ is a hydrogenatom, a chlorine atom or a bromine atom; provided that at least one ofU⁴ or U⁵ is a hydrogen atom.
 11. A process for preparing a compound offormula (I) according to claim 1 comprising the step of performing adiazotation of a compound of formula (X) or a salt thereof followed byan aromatic substitution:

wherein R¹, R², R³, R⁴, R⁵ and R⁶ are as recited in claim 1; U⁶ is anamino group, a chlorine atom or a bromine atom; U⁷ is an amino group, achlorine atom or a bromine atom; provided that at least one of U⁶ or U⁷is an amino group.